Referenced in: none

Automatically associated channels: ClC1 , ClC4 , Kv2.1

Title: A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.

Authors: S Nagamitsu, T Matsuura, M Khajavi, R Armstrong, C Gooch, Y Harati, T Ashizawa

Journal, date & volume: Neurology, 2000 Dec 12 , 55, 1697-703

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/11113225

Abstract