Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy

Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy

OBJECTIVE: To study the phenotypes and proline-rich transmembrane protein 2 (PRRT2) mutations in families with benign familial infantile epilepsy (BFIE)

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 52(2014), 11 vom: 13. Nov., Seite 806-11
Auteur principal: Yang, Xiaoling (Auteur)
Autres auteurs: Zhang, Yuehua, Xu, Xiaojing, Yu, Xiaoli, Zhang, Xiuju, Yang, Zhixian, Wang, Shuang, Wu, Ye, Liu, Xiaoyan, Wu, Xiru
Format: Article
Langue:Chinese
Publié: 2014
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Journal Article Membrane Proteins Nerve Tissue Proteins PRRT2 protein, human