ATP1A3 gene mutations in patients with alternating hemiplegia of childhood

OBJECTIVE: To analyze the ATP1A3 mutations in patients with alternating hemiplegia of childhood (AHC) and recognize its value in diagnosing atypical cases

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 53(2015), 11 vom: 05. Nov., Seite 835-9
Auteur principal: Yang, Xiaoling (Auteur)
Autres auteurs: Zhang, Yuehua, Yuan, Dawei, Xu, Xiaojing, Li, Shupin, Wei, Liping, Wu, Ye, Xiong, Hui, Liu, Xiaoyan, Bao, Xinhua, Jiang, Yuwu, Wu, Xiru
Format: Article
Langue:Chinese
Publié: 2015
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Journal Article ATP1A3 protein, human Sodium-Potassium-Exchanging ATPase EC 7.2.2.13