Referenced in: none

Automatically associated channels: ClC1 , ClC4 , Kir2.3

Title: Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenita.

Authors: R Brugnoni, S Galantini, P Confalonieri, M R Balestrini, F Cornelio, R Mantegazza

Journal, date & volume: Hum. Mutat., 1999 Nov , 14, 447

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/10533075

Abstract