Referenced in: none

Automatically associated channels: Nav1.4

Title: Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.

Authors: E Plassart, J Reboul, C S Rime, D Recan, P Millasseau, B Eymard, J Pelletier, C Thomas, F Chapon, C Desnuelle

Journal, date & volume: Eur. J. Hum. Genet., 1994 , 2, 110-24

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/8044656

Abstract