Referenced in: none

Automatically associated channels: Nav1.1

Title: Novel SCN1A frameshift mutation with absence of truncated Nav1.1 protein in severe myoclonic epilepsy of infancy.

Authors: Erin J McArdle, Jennifer D Kunic, Alfred L George

Journal, date & volume: Am. J. Med. Genet. A, 2008 Sep 15 , 146A, 2421-3

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18680191

Abstract