Referenced in: none

Automatically associated channels: Nav1.4 , Slo1

Title: A novel mutation in SCN4A causes severe myotonia and school-age-onset paralytic episodes.

Authors: Harumi Yoshinaga, Shunichi Sakoda, Jean-Marc Good, Masanori P Takahashi, Tomoya Kubota, Eri Arikawa-Hirasawa, Tomohiko Nakata, Kinji Ohno, Tetsuro Kitamura, Katsuhiro Kobayashi, Yoko Ohtsuka

Journal, date & volume: J. Neurol. Sci., 2012 Apr 15 , 315, 15-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22257501

Abstract