Referenced in: none

Automatically associated channels: Nav1.1

Title: Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants.

Authors: Renzo Guerrini, Melania Falchi

Journal, date & volume: Dev Med Child Neurol, 2011 Apr , 53 Suppl 2, 11-5

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21504426

Abstract