Referenced in: none

Automatically associated channels: Nav1.4 , Slo1

Title: A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.

Authors: Karima Habbout, Hugo Poulin, Francois Rivier, Serena Giuliano, Damien Sternberg, Bertrand Fontaine, Bruno Eymard, Raul Juntas Morales, Bernard Echenne, Louise King, Michael G Hanna, Roope Männikkö, Mohamed Chahine, Sophie Nicole, Saïd Bendahhou

Journal, date & volume: Neurology, 2016 Jan 12 , 86, 161-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26659129

Abstract