Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia

Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia

OBJECTIVE: To investigate the clinical features and proline-rich transmembrane protein 2 (PRRT2) gene mutation in patients with paroxysmal kinesigenic dyskinesia (PKD)

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 53(2015), 8 vom: 30. Aug., Seite 621-5
Auteur principal: Yang, Xiaoling (Auteur)
Autres auteurs: Zhang, Yuehua, Xu, Xiaojing, Yang, Zhixian, Wang, Shuang, Wu, Ye, Wu, Xiru
Format: Article
Langue:Chinese
Publié: 2015
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Journal Article Membrane Proteins Nerve Tissue Proteins PRRT2 protein, human