A new case of autosomal dominant myotonia associated with...

A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification

D. Ferriby, T. Stojkovic, D. Sternberg, J.-F. Hurtevent, J.-P. Hurtevent, P. Vermersch

How much do you like this book?

What’s the quality of the file?

Download the book for quality assessment

What’s the quality of the downloaded files?

Volume:

Year:

2006

Language:

english

DOI:

10.1016/j.nmd.2006.01.015

File:

PDF, 181 KB

english, 2006

Conversion to is in progress

Conversion to is failed