Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome

Human Molecular Genetics 2015 24:1; pp. 243–250; doi: 10.1093/hmg/ddu442

The authors apologize for the errors made in the second part of the Result section. In all cases, the mutation should be c.23G>T rather than c.23G>A.