PubMed 18807109
Referenced in: none
Automatically associated channels: ClC1 , ClC4
Title: High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.
Authors: T Suominen, B Schoser, O Raheem, S Auvinen, M Walter, R Krahe, H Lochmüller, W Kress, B Udd
Journal, date & volume: J. Neurol., 2008 Nov , 255, 1731-6
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18807109
Abstract