Referenced in: none

Automatically associated channels: Cav2.1 , Nav1.5 , Slo1

Title: The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

Authors: Kaate R J Vanmolkot, Elena Babini, Boukje de Vries, Anine H Stam, Tobias Freilinger, Gisela M Terwindt, Lisa Norris, Joost Haan, Rune R Frants, Nabih M Ramadan, Michel D Ferrari, Michael Pusch, Arn M J M Van Den Maagdenberg, Martin Dichgans

Journal, date & volume: Hum. Mutat., 2007 May , 28, 522

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/17397047

Abstract