Abstract

Episodic ataxia type 1 (EA1) is a rare autosomal dominant disorder characterized by brief episodes of ataxia associated with continuous interattack myokymia. Point mutations in the human voltage-gated potassium channel (Kv1.1) gene on chromosome 12p13 have recently been shown to associate with EA1. A Scottish family with EA1 harbouring a novel mutation in this gene is reported. Of the five affected individuals over three generations, two had partial epilepsy in addition to EA1. The detailed clinical, electrophysiological and molecular genetic findings are presented. The heterozygous point mutation is located at nucleotide position 677 and results in a radical amino acid substitution at a highly conserved position in the second transmembrane domain of the potassium channel. Functional studies indicated that mutant subunits exhibited a dominant negative effect on potassium channel function and would be predicted to impair neuronal repolarization. Potassium channels determine the excitability of neurons and blocking drugs are proconvulsant. A critical review of previously reported EA1 families shows an over-representation of epilepsy in family members with EA1 compared with unaffected members. These observations indicate that this mutation is pathogenic and suggest that the epilepsy in EA1 may be caused by the dysfunctional potassium channel. It is possible that such dysfunction may be relevant to other epilepsies in man.

Introduction

Episodic ataxia type 1 (EA1, MIM 160120) is a rare autosomal dominant disorder in which patients develop sudden episodes of ataxia precipitated by movement, startle or emotion and which last for a time ranging from seconds to minutes (Van Dyke et al., 1975). In addition, there is continuous myokymia which may be clinically evident or only detectable by EMG. In episodic ataxia type 2 (EA2, MIM 108500) affected individuals experience prolonged attacks of ataxia lasting hours, often accompanied by nausea, vomiting and headache but not associated with myokymia. EA2 subjects frequently develop a progressive cerebellar ataxia accompanied by cerebellar atrophy (Gancher et al., 1986). Point mutations in the voltage-gated potassium channel gene (Kv1.1) on chromosome 12p13 have been shown to be associated with EA1 while mutations in the P/Q-type voltage-gated calcium channel gene (CACLNA4) on chromosome 19p13 underlie EA2 (Browne et al., 1994; Litt et al., 1994; Ophoff et al., 1996). There is increasing evidence from animal studies that dysfunctional ion channels are responsible for the commonest episodic neurological disorder, epilepsy (Noebels, 1996). We describe a Scottish family with EA1 in whom a point mutation has been identified in the voltage-gated potassium channel gene Kv1.1. In addition to EA1, two members had partial epilepsy and we discuss the possibility that dysfunction of this channel is associated with epilepsy in humans.

Subjects and methods

Clinical study

EMG was performed on four patients (Synergy EMG/EP; Medelec, UK). EEG was carried out on four individuals (Nicolet Voyageur 1.4; Nicolet Biomedical, Madison, Wis., USA). Three individuals had a CT brain scan and one had a 1.5 T MRI brain scan. Video recordings were made of all individuals who were examined. Ataxic episodes were induced and recorded on videotape in two cases.

Video EEG (Oxford Medilog System 9200, Oxford, UK with Video Interface Processor; Oxford Medical Systems, Oxford, UK) was performed on two patients, capturing epileptic seizures in one and an ataxic episode in another.

Genetic study

In order to screen control chromosomes and other family members for the C→G point mutation at position 677, a mismatch PCR technique was employed since this mutation neither created nor abolished a natural restriction site. This PCR reaction creates a restriction site for DdeI only in the presence of a G nucleotide at position 677. The two primers used were the forward (mismatch) primer (nucleotide positions 647–676): 5′-TCTTCACAGACCCCTTCTTCATCGTGCTAA3′ (mismatch nucleotides shown bold underlined), and the reverse primer (nucleotide positions 806–787): 5′-AGGGTGATGAAATAAGGAAT3.

The wild-type sequence between positions 672 and 677 is GGAAAC. Following amplification with the mismatch primer, the following sequence is generated in the wild type: GCTAAC. In the presence of the C677G mutation the sequence GCTAAG is generated, which contains the recognition site for DdeI (C/TNAG). The conditions for the mismatch PCR were identical to those for the PCR described above. After digestion with DdeI according to the manufacturer's recommendations, the fragments were separated on a 3.2% agarose gel stained with ethidium bromide and visualized on an ultraviolet light-box.

Functional study

Human Kv1.1 wild-type and mutant genes were amplified using PCR on genomic DNA extracted from a blood sample of one of the affected family members. PCR products were subcloned into the vector pSGEM (courtesy of Dr M. Hollmann, Göttingen, Germany), which provides 5′- and 3′-untranslated regions from the Xenopus β-globin gene, flanking a polylinker with multiple restriction sites. Wild-type and mutant clones were completely sequenced on both stands and then transcribed in vitro using T7-RNA polymerase (Boehringer Mannheim, Germany). Xenopus oocytes were defolliculated manually after collagenase treatment and injected with 0.2–1.4 ng mRNA using a Nanoject automatic injector (Drummond). Injected oocytes were kept in Barth's medium for 3–5 days at 18°C prior to recording in a solution containing (in mM): NaCl, 115; KCl, 2.5; CaCl2, 1.8; HEPES, 10; pH = 7.4. Two-electrode voltage-clamp recording was performed at 22°C using a GeneClamp 500 amplifier, and data were acquired and analysed using pClamp6 (Axon Instruments, Foster City, Calif., USA). Leak and capacitative currents were subtracted applying a -P/4 protocol.

Results

Case reports

Case III2

At 20 months the patient developed irritability and swelling of his hands and feet. He had clenched fists and flexion of the toes. The dorsum of his hands and feet appeared swollen and oedematous and he refused to walk. Investigations for renal and joint disorders were negative and the problems resolved within a few days.

Case I1

The 50-year-old maternal grandmother of the proband has had symptoms of intermittent ataxia since early childhood. They are precipitated by sudden movements, exercise, anxiety or loud noises, or occur spontaneously and last seconds to a few minutes. During the episodes she becomes ataxic, has dysarthria but retains full consciousness. Phenonobarbitone therapy as a child was not helpful. She attended a school for children with mild to moderate learning difficulties. Clinical examination is normal apart from periorbital and finger myokymia. Acetazolamide was unhelpful.

Case II2

This 31-year-old male was noted to have postural abnormalities of his upper and lower limbs at the age of 3 months when admitted with bronchiolitis. His wrists were flexed, the thumbs were adducted across his palms and his feet were held in equinovarus. There was no spasticity on examination. He was treated with splints. During this acute illness he developed transient oedema of his extremities. He was noted to have twitching of his eyelids but an EEG was normal. At 5 months he had surgery for a strangulated inguinal hernia. He walked at 14 months and his foot deformity had resolved, but he had a continued tendency to adduct his thumbs across his palms.

Case II4

This 30-year-old woman has EA1 and epilepsy. She presented in early infancy with more prominent postural deformities of her limbs than in her brother. Her wrists were flexed to 50°, her thumbs were held in partial adduction, her knees were flexed to 20° and her feet were in an equinovarus posture. Serum creatine phosphokinase was normal. An EEG in infancy was normal. A diagnosis of atypical familial arthrogryposis was made. She also required surgery for an inguinal hernia. She walked late at 2 years of age and by 3 years the postural abnormalities had almost completely resolved. At the age of 9 years she was diagnosed as having stage IV Hodgkin's disease. She responded to chemotherapy and localized radiotherapy and since then she has been disease-free.

At the ages of 9 and 10 years she began to have epileptic seizures and episodic ataxia, respectively. The clinical features of the seizures suggest that they are complex partial followed by secondary generalization. There is no warning and the onset involves turning the head to the right accompanied by impaired awareness lasting up to 30 s followed by a generalized tonic clonic seizure. EEG and CT brain were normal at the age of 9 years. The ataxic episodes are clearly distinguished from the seizures and are similar to those described in her mother and brother. Consciousness is fully preserved. Neither the seizures nor the ataxic episodes have responded to phenytoin or sodium valproate. On examination she has periorbital and finger myokymia. EEG in 1997 was normal apart from prominent muscle activity artefact.

Genetic results

Direct DNA sequence analysis of all 1488 bp of the Kv1.1 gene revealed three heterozygous changes. These were C677G, C684T and C804G. In addition, our data indicate that the consensus nucleotide at position 1355 is C and not A (Browne et al., 1994). The C684G and C804G changes were silent and were observed in 5% of control chromosomes analysed. However, the C→G transition at position 677 was not detected in 200 control chromosomes and segregated with the disease in the family, suggesting that it is likely to be pathogenic (Figs 1 and 6). Furthermore, this mutation results in a radical amino acid substitution (threonine→ arginine) at position 226, a highly conserved position in the second transmembrane segment of the channel, and is therefore likely to have functional consequences (Figs 7 and 8).

Discussion

Clinical features and investigations

We have reported a family with the rare autosomal dominant disorder EA1 in which two individuals have epilepsy. As in other paroxysmal conditions due to ion channel dysfunction, there was a long delay in making the correct diagnosis. This was appreciated only when the family history became apparent. A factitious disorder had been considered in case II2. The initial presentation with postural abnormalities in infancy in all cases except case I1 has been described in one family previously (Hanson et al., 1977). This is presumed to be a manifestation of the continuous muscle fibre activity at this age. Inguinal hernias were present in two siblings in generation II, and these may also be secondary to myokymia of the abdominal wall musculature. Case II4 had the most severe postural deformities and a diagnosis of arthrogryposis was considered. It is notable that the postural deformities gradually resolve and are not a significant long-term problem. It is therefore important to avoid surgical intervention. The postural abnormalities were more pronounced during acute illnesses in three of our cases. This may be due to acid–base or electrolyte imbalance exacerbating ion channel dysfunction. The age at onset of the ataxic episodes was between 2 and 4 years except in case II4, whose attacks started at the age of 9 years. The ataxia was precipitated by similar stimuli of sudden movement, startle or exercise in each case. The episodes never lasted for more than a few minutes. In contrast to EA2, eye movements remain normal during the attacks and there is no evidence of progressive interictal cerebellar dysfunction. Myokymia was present in all individuals. Clinically this was evident as small semirhythmic irregular lateral finger movements and rippling of muscles below the eyelids.

The most helpful clinical investigation was EMG, which showed typical rhythmic continuous motor unit activity in all individuals (Fig. 3). The observation of a continuous rhythmic muscle discharge artefact on EEG recordings was also a clue to the correct diagnosis (Fig. 4). The muscle activity on the EEG became more prominent with hyperventilation, which may reflect the effect of pH or CO2 changes on ion channel function. Acetazolamide, a carbonic anhydrase inhibitor, which may be effective in reducing ataxic episodes in some individuals, has been partly effective in only one of our patients (Lubbers et al., 1995). The precise therapeutic mechanism of acetazolamide is not known. It may act by increasing the CO2 concentration in the vicinity of the ion channel, causing hyperpolarization of the cell membrane and thereby reducing neuronal excitability (Brunt et al., 1990). Some of the cases reported here had a partial response to carbamazepine. Other reported cases have responded to antiepileptic medication such as carbamazepine, phenytoin and phenobarbitone. These observations indicate that the treatment response in EA1 varies, and it is possible that it may be mutation-specific.

Molecular genetic and functional studies

In view of the reported association between EA1 and mutations in the human voltage-gated potassium channel gene Kv1.1, we sequenced the entire gene from genomic DNA in the proband. The heterozygous C→G change identified at position 677 had characteristics that suggested it was likely to be of pathogenic relevance. Further evidence in favour of pathogenicity was obtained from expression studies. These indicated that the mutant allele is correctly translated and processed to the cell membrane, but that it yields currents with a largely reduced amplitude compared with wild-type channels. In co-expression studies the mutant allele seemed to dominate over the wild type with respect to current amplitude. Thus, heterotetrameric channels, as might be expressed in neurons of heterozygous patients, would be predicted to have a reduced potassium efflux during action potentials. A similar degree of current amplitude reduction was observed in co-expression studies (ratio 1 : 1) of another pathogenic Kv1.1 point mutation at amino acid position 408 (Adelman et al., 1995). Such studies have shown a greater degree of current amplitude reduction in association with other pathogenic Kv1.1 mutations (Adelman et al., 1995). However, the relationship between the degree of current amplitude reduction in such co-expression studies and functional impairment of neuronal repolarization is unknown. It is possible that even a relatively small reduction in potassium current amplitude could disturb the complex equilibrium between a number of conductances in the membrane of affected neurons and account for a delay in repolarization, thereby facilitating the generation and spread of action potentials. This delayed repolarization is likely to be the basis of the neuromyotonia and episodes of ataxia. In addition, it is possible that such a defect in neuronal repolarization could lower the seizure threshold. To date, nine point mutations in Kv1.1 have been reported in association with the EA1 phenotype. Expression studies have identified two broad mechanisms by which such mutations induce channel dysfunction and would be predicted to impair neuronal repolarization. The first group of mutations form homomeric channels with altered gating properties. The second group of mutations do not produce functional homomeric channels but co-expression studies with wild-type channels indicate that these mutations may induce a dominant negative effect (Adelman et al., 1995; Zerr et al., 1998a, b).

Possible relationship between EA1 and epilepsy

This is the eleventh family with EA1 to be reported. Within this group, 90 individuals have been identified with the phenotype of episodic ataxia and myokymia (Van Dyke et al., 1975; Hanson et al., 1977; Gancher and Nutt 1986; Brunt and Van Weerden 1990; Vaamonde et al., 1991; Browne et al., 1994; Browne et al., 1995; Lubbers et al., 1995; Comu et al., 1996). Of these, eight individuals from three families, including our own, are reported to have epilepsy. In addition we have recently identified a further family with a previously undescribed Kv1.1 mutation in which members affected with EA1 also have epilepsy (R. Liguori and M. G. Hanna, unpublished observations). In all these families none of the unaffected family members are reported to have epilepsy. Table 2 summarizes the published information. These data suggest that patients with EA1 are ten times more likely to develop epilepsy than normal individuals. Assuming a general population risk of epilepsy of 1 : 200, the relative risk of epilepsy in EA1 is 17.8 (95% confidence interval 2.3–140.4). In all reported cases the epileptic seizures were easily distinguished from the ataxic episodes. The seizure type was described only in one previous report, and was a generalized motor seizure' (Van Dyke et al., 1975). The first case (III2) with EA1 and epilepsy that we describe is difficult to classify using standard criteria (Commission on Classification and Terminology of the International League Against Epilepsy, 1989). His epilepsy is best described as a benign partial seizure disorder of infancy. He had onset of complex partial seizures in the neonatal period, normal interictal EEG, no identifiable lesion on imaging, an excellent response to antiepileptic medication and normal subsequent development (Okumura et al., 1996). In contrast, case II4 had clinical features which were compatible with a partial epilepsy with secondary generalization. It is possible that that the mutation we have identified causes the different epilepsy phenotypes in our family and that other mutations in Kv1.1 may be associated with epilepsy. In support of this suggestion, a mouse knockout for Kv1.1 has been described to have a lethal epilepsy phenotype (Smart et al., 1999). It is also recognized that drugs which block Kv1.1 are proconvulsant in humans (Newsom-Davis, 1993; Morales-Villagran et al., 1996). The expression of Kv1.1 has not been studied in man, but in rats it is widely expressed throughout the nervous system, including the hippocampus (Beckh et al., 1990). It remains to be explained why only two of the five members of our family developed epilepsy. It is possible that other factors, which may be genetic or environmental, could be important in influencing the phenotype. In other ion channel disorders it is recognized that the same point mutation can be associated with phenotypic heterogeneity (Bulman, 1997).

Recently two new potassium genes have been cloned, and direct evidence has been provided that mutations in these genes are associated with epilepsy (Biervert et al., 1998; Charlier et al., 1998; Singh et al., 1998). It is of interest that in both cases these seizures were similar to those observed in case III2. They were benign seizures in the neonatal period which resolved and were classified as benign neonatal familial seizures.

In conclusion, we described a novel mutation in Kv1.1 in a family with episodic ataxia type I. Functional studies have shown that this mutation reduces potassium channel current amplitude in a dominant negative fashion. This is likely to be the basis of the neuromyotonia and episodic ataxia. We provide some evidence that dysfunction of this channel may be associated with epilepsy in man.

Table 1

Three oglionucleotide primer pairs used to amplify the Kv1.1 gene

 (1) Forward (nucleotides 1–20) 5′-ATGACGGTGATGTCTGGGGA-3′ Reverse (nucleotides 550–531) 5′-AGATGACGATGGAGATGAGG-3′ (2) Forward (nucleotides 481–500) 5′-GAGAGCTCGGGGCCCGCCAG-3′ Reverse (nucleotides 983–974) 5′-AAAGATGAGCAGCCCTAGCT-3′ (3) Forward (nucleotides 931–950) 5′-GGCCTCCAGATCCTGGGCCA-3′ Reverse (nucleotides 1469–1488) 5′-TTAAACATCGGTCAGTAGCT-3′
 (1) Forward (nucleotides 1–20) 5′-ATGACGGTGATGTCTGGGGA-3′ Reverse (nucleotides 550–531) 5′-AGATGACGATGGAGATGAGG-3′ (2) Forward (nucleotides 481–500) 5′-GAGAGCTCGGGGCCCGCCAG-3′ Reverse (nucleotides 983–974) 5′-AAAGATGAGCAGCCCTAGCT-3′ (3) Forward (nucleotides 931–950) 5′-GGCCTCCAGATCCTGGGCCA-3′ Reverse (nucleotides 1469–1488) 5′-TTAAACATCGGTCAGTAGCT-3′
Table 2

Epilepsy and EA1

Author Sex Age at onset Seizure description EEG features Response to medication Mutation
– = data not reported.
Van Dyke et al. (1975) 21 years Generalized motor seizures Paroxysmal 6/s slowing Phenytoin (partial) Phe184Cyst
– – – – Phe184Cyst
– – – – Phe184Cyst
Brunt and van Weerden (1990) – – Abnormal' Phenobarbitone Val174Phe
– – Abnormal' Phenobarbitone Val174Phe
– – Abnormal' Phenobarbitone Val174Phe
This report 9 years Partial with generalization Normal Phenytoin, no response to valproate Thr226Arg
7 weeks Complex partial Normal interictal Carbamazepine Thr226Arg
Ictal focal spike slow wave
Author Sex Age at onset Seizure description EEG features Response to medication Mutation
– = data not reported.
Van Dyke et al. (1975) 21 years Generalized motor seizures Paroxysmal 6/s slowing Phenytoin (partial) Phe184Cyst
– – – – Phe184Cyst
– – – – Phe184Cyst
Brunt and van Weerden (1990) – – Abnormal' Phenobarbitone Val174Phe
– – Abnormal' Phenobarbitone Val174Phe
– – Abnormal' Phenobarbitone Val174Phe
This report 9 years Partial with generalization Normal Phenytoin, no response to valproate Thr226Arg
7 weeks Complex partial Normal interictal Carbamazepine Thr226Arg
Ictal focal spike slow wave
Fig. 1

Upper panel. Pertinent part of the pedigree of the EA1/epilepsy family. Filled symbols indicate individuals with EA1. The two individuals with epilepsy are indicated by Ep'. The lower panel shows an agarose gel containing the DNA fragments following digestion with the restriction endonuclease DdeI. Normal individuals have the upper band only (159 bp undigested mismatch PCR product as described under Subjects and methods) as shown for cases II1 and II3 (cases I2 and II5 did not harbour the mutation; data not shown). The presence of the C677G mutation introduces a restriction site in the affected individuals (cases I1, II2, II4, III1, III2), and two bands are visible in these cases. These are the upper band, which is the undigested 159-bp product, and the lower band, which is the larger 131-bp product of digestion. The smaller 28-bp product of digestion is not shown. Lane 1, case III1; lane 2, case II1; lane 3, case II2; lane 4, case III2; lane 5, case II3; lane 6, case I1; lane 7, case II4. The proband (case III2) is indicated by an arrow.

Fig. 1

Upper panel. Pertinent part of the pedigree of the EA1/epilepsy family. Filled symbols indicate individuals with EA1. The two individuals with epilepsy are indicated by `Ep'. The lower panel shows an agarose gel containing the DNA fragments following digestion with the restriction endonuclease DdeI. Normal individuals have the upper band only (159 bp undigested mismatch PCR product as described under Subjects and methods) as shown for cases II1 and II3 (cases I2 and II5 did not harbour the mutation; data not shown). The presence of the C677G mutation introduces a restriction site in the affected individuals (cases I1, II2, II4, III1, III2), and two bands are visible in these cases. These are the upper band, which is the undigested 159-bp product, and the lower band, which is the larger 131-bp product of digestion. The smaller 28-bp product of digestion is not shown. Lane 1, case III1; lane 2, case II1; lane 3, case II2; lane 4, case III2; lane 5, case II3; lane 6, case I1; lane 7, case II4. The proband (case III2) is indicated by an arrow.

Fig. 2

EEG of case III2 during complex partial epileptic seizure. Right temporal sharp and slow waves generalize to involve the right hemisphere.

Fig. 2

EEG of case III2 during complex partial epileptic seizure. Right temporal sharp and slow waves generalize to involve the right hemisphere.

Fig. 3

Surface EMG, case III2. Upper panel: continuous motor unit activity, rhythmically occurring singlets and duplets with variation in spike frequency. Lower panel: spike and shadow potentials.

Fig. 3

Surface EMG, case III2. Upper panel: continuous motor unit activity, rhythmically occurring singlets and duplets with variation in spike frequency. Lower panel: spike and shadow potentials.

Fig. 4

Normal EEG in case II2 shows rhythmic EMG (10/s) over the temporal region.

Fig. 4

Normal EEG in case II2 shows rhythmic EMG (10/s) over the temporal region.

Fig. 5

Case III1, aged 8 months. Fists are clenched, knees are flexed and feet held in plantar flexion as a result of the continuous muscle fibre activity.

Fig. 5

Case III1, aged 8 months. Fists are clenched, knees are flexed and feet held in plantar flexion as a result of the continuous muscle fibre activity.

Fig. 6

Electropherogram of Kv1.1 gene DNA sequence. (Upper panel) Wild-type DNA sequence. (Lower panel) Sequence from the proband (case III2). The silent polymorphism at position 684 (indicated by X) is present in both the control and the proband. The C→G mutation at position 677 indicated by the double arrowhead is present only in the proband.

Fig. 6

Electropherogram of Kv1.1 gene DNA sequence. (Upper panel) Wild-type DNA sequence. (Lower panel) Sequence from the proband (case III2). The silent polymorphism at position 684 (indicated by X) is present in both the control and the proband. The C→G mutation at position 677 indicated by the double arrowhead is present only in the proband.

Fig. 7

Schematic representation of one subunit of Kv1.1. The site of the T226R amino acid substitution resulting from the C677G point mutation in the second transmembrane domain is indicated.

Fig. 7

Schematic representation of one subunit of Kv1.1. The site of the T226R amino acid substitution resulting from the C677G point mutation in the second transmembrane domain is indicated.

Fig. 8

Table illustrating that threonine at position 226 (arrow) is highly conserved through evolution.

Fig. 8

Table illustrating that threonine at position 226 (arrow) is highly conserved through evolution.

Fig. 9

Amplitude histogram of whole-cell currents in Xenopus laevis oocytes. Currents of cells injected with wild type (Wt) were compared with cells injected with mutant (T226R) and with uninjected cells. Cells were voltage-clamped at –100 mV and current amplitudes were measured at the end of a 350-ms pulse to +40 mV. Error bars indicate standard deviation (n is between 5 and 9). The concentration of mRNA was determined by ethidium bromide staining and spectrophotometry to adjust the ratio of mutant to wild-type subunits. Oocytes injected with mutant mRNA show a marked reduction in voltage-activated currents. Increasing amounts of mutant mRNA were injected in the presence of a constant amount of wild-type mRNA. A progressive decline in voltage-activated current was obtained as the amount of mutant mRNA increased.

Fig. 9

Amplitude histogram of whole-cell currents in Xenopus laevis oocytes. Currents of cells injected with wild type (Wt) were compared with cells injected with mutant (T226R) and with uninjected cells. Cells were voltage-clamped at –100 mV and current amplitudes were measured at the end of a 350-ms pulse to +40 mV. Error bars indicate standard deviation (n is between 5 and 9). The concentration of mRNA was determined by ethidium bromide staining and spectrophotometry to adjust the ratio of mutant to wild-type subunits. Oocytes injected with mutant mRNA show a marked reduction in voltage-activated currents. Increasing amounts of mutant mRNA were injected in the presence of a constant amount of wild-type mRNA. A progressive decline in voltage-activated current was obtained as the amount of mutant mRNA increased.

We wish to thank Dr A. Jamieson, Department of Medical Genetics, and Ms Jean Hyslop, Department of Medical Illustration, Royal Hospital for Sick Children, for their help in preparing this manuscript. Financial support from the Brain Research Trust, the Medical Research Council of Great Britain and Northern Ireland and the Wellcome Trust is gratefully acknowledged.

References

Adelman JP, Bond CT, Pessia M, Maylie J. Episodic ataxia results from voltage-dependent potassium channels with altered functions.
Neuron

1995
;
15
:
1449
–54.
Beckh S, Pongs O. Members of the RCK potassium channel family are differentially expressed in the rat nervous system.
EMBO J

1990
;
9
:
777
–82.
Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, et al. A potassium channel mutation in neonatal human epilepsy.
Science

1998
;
279
:
403
–6.
Browne DL, Gancher ST, Nutt JG, Brunt ER, Smith EA, Kramer P, et al. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene KCNA1 [see comments].
Nat Genet

1994
;
8
:
136
–40. Comment in: Nat Genet 1994; 8: 111–2.
Browne DL, Brunt ER, Griggs RC, Nutt JG, Gancher ST, Smith EA, et al. Identification of two new KCNA1 mutations in episodic ataxia/myokymia families.
Hum Mol Genet

1995
;
4
:
1671
–2.
Brunt ER, van Weerden TW. Familial paroxysmal kinesigenic ataxia and continuous myokymia.
Brain

1990
;
113
:
1361
–82.
Bulman DE. Phenotype variation and newcomers in ion channel disorders.[Review].
Hum Mol Genet

1997
;
6
:
1679
–85.
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, et al. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family [see comments].
Nat Genet

1998
;
18
:
53
–5. Comment in: Nat Genet 1998; 18: 6–8.
Commission on Classification and Terminology of the International League Against Epilepsy. Proposal for revised classification of epilepsies and epileptic syndromes.
Epilepsia

1989
;
30
:
389
–99.
Comu S, Giuliani M, Narayanan V. Episodic ataxia and myokymia syndrome: a new mutation of potassium channel gene Kv1.1.
Ann Neurol

1996
;
40
:
684
–7.
Gancher ST, Nutt JG. Autosomal dominant episodic ataxia: a heterogeneous syndrome.
Mov Disord

1986
;
1
:
239
–53.
Hanson PA, Martinez LB, Cassidy R. Contractures, continuous muscle discharges, and titubation.
Ann Neurol

1977
;
1
:
120
–4.
Litt M, Kramer P, Browne D, Gancher S, Brunt ERP, Root D, et al. A gene for episodic ataxia/myokymia maps to chromosome 12p13.
Am J Hum Genet

1994
;
55
:
702
–9.
Lubbers WJ, Brunt ERP, Scheffer H, Litt M, Stulp R, Browne DL, et al. Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide.
J Neurol Neurosurg Psychiatry

1995
;
59
:
400
–5.
Morales-Villagran A, Urena-Guerrero ME, Tapia R. Protection by NMDA receptor antagonists against seizures induced by intracerebral administration of 4-aminopyridine.
Eur J Pharmacol

1996
;
305
:
87
–93.
Newsom-Davis J. The management of myasthenic syndromes.
Prescribers J

1993
;
33
:
210
–1.
Noebels JL. Targeting epilepsy genes. [Review].
Neuron

1996
;
16
:
241
–4.
Okumura A, Hayakawa F, Kuno K, Watanabe K. Benign partial epilepsy in infancy.
Arch Dis Child

1996
;
74
:
19
–21.
Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the calcium channel gene CACNL1A4.
Cell

1996
;
87
:
543
–52.
Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, et al. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns [see comments].
Nat Genet

1998
;
18
:
25
–9. Comment in: Nat Genet 1998; 18: 6–8.
Smart SL, Lopanstev V, Zhang CL, Robbins CA, Wang H, Chiu ST, et al. Deletion of the Kv1.1 potassium channel causes epilepsy in mice.
Neuron

1998
;
20
:
809
–19.
Vaamonde J, Artieda J, Obeso JA. Hereditary paroxysmal ataxia with neuromyotonia.
Mov Disord

1991
;
6
:
180
–2.
Van Dyke DH, Griggs RC, Murphy MJ, Goldstein MN. Hereditary myokymia and periodic ataxia.
J Neurol Sci

1975
;
25
:
109
–18.
Zerr P, Adelman JP, Maylie J. Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency.
J Neurosci

1998
;
18
:
2842
–8.
Zerr P, Adelman JP, Maylie J. Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel.
FEBS Lett

1998
;
431
:
461
–4.