Genetic and clinical analysis of children with early-onset epilepsy encephalopathy caused by KCNT1 gene mutation

Objective: To study the mutational characteristics of KCNT1 and its clinical features in children with early-onset epileptic encephalopathy. Methods: Retrospective analysis of clinical data of 175 children with early onset epilepsy from the Department of Pediatrics at Peking University First Hospita...

Description complète

Détails bibliographiques

Publié dans:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 56(2018), 11 vom: 02. Nov., Seite 824-828
Auteur principal:	Chen, Y (Auteur)
Autres auteurs:	Bao, X H, Zhang, Q P, Wang, J P, Wen, Y X, Yu, S J, Zhao, Y
Format:	Article en ligne
Langue:	Chinese
Publié:	2018
Accès à la collection:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:	Journal Article Epilepsy Genes Quinidine KCNT1 protein, human Nerve Tissue Proteins Potassium Channels Potassium Channels, Sodium-Activated