Spectrum of SCN8A-Related Epilepsy

Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features

Détails bibliographiques
Publié dans:Pediatric neurology briefs. - 1997. - 29(2015), 2 vom: 01. Feb., Seite 16
Auteur principal: Morgan, Lindsey A (Auteur)
Autres auteurs: Millichap, John J
Format: Article en ligne
Langue:English
Publié: 2015
Accès à la collection:Pediatric neurology briefs
Sujets:Journal Article Dravet Syndrome Epileptic Encephalopathies SCN8A Voltage Gated Sodium Channels
Description
Résumé:Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features
Description:Date Completed 02.03.2016
Date Revised 29.09.2020
published: Print
Citation Status PubMed-not-MEDLINE
ISSN:1043-3155
DOI:10.15844/pedneurbriefs-29-2-7