PubMed 17717708
Referenced in: none
Automatically associated channels: ClC1 , ClC4
Title: Novel human pathological mutations. Gene symbol: CLCN1. Disease: myotonia congenita, autosomal recessive.
Authors: Fernando Morales, Patricia Cuenca, Gerardo del Valle, Melissa Vásquez, Roberto Brian, Mauricio Sittenfeld, Keith Johnson, Xi Lin, Tetsuo Ashizawa
Journal, date & volume: Hum. Genet., 2007 Nov , 122, 413
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/17717708
Abstract