Referenced in: none

Automatically associated channels: Kv1.1 , Nav1.4

Title: A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A.

Authors: S Rajakulendran, S V Tan, E Matthews, S E Tomlinson, R Labrum, R Sud, D M Kullmann, S Schorge, M G Hanna

Journal, date & volume: Neurology, 2009 Sep 22 , 73, 993-5

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19770477

Abstract