Human Molecular Genetics   12 , 1337–1348 (2003)

The characterisation of a dystrophin gene rearrangement associated with X-linked dilated cardiomyopathy and used for some of the studies in the manuscript by Nasim et al. has been published:

Gualandi, G., Rimessi, P., Cardazzo, B., Toffolatti, L., Dunckley, M.G., Calzolari, E., Patarnello, T., Muntoni, F. and Ferlini, A. (2003) Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormality. Gene , 311 , 23–31.