Article
[Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].
Zhonghua er ke za zhi = Chinese journal of pediatrics - 1 Aug 2015
Yang Xiaoling, Zhang Yuehua, Xu Xiaojing, Yang Zhixian, Wang Shuang, Wu Ye, Wu Xiru
Abstract excerpt
OBJECTIVE: To investigate the clinical features and proline-rich transmembrane protein 2 (PRRT2) gene mutation in patients with paroxysmal kinesigenic dyskinesia (PKD). METHOD: Clinical information was collected at Peking University First Hospital from January 2004 to July 2014. In total, 10 patients with PKD were recruited, and all were males. Among them, four patients were the probands from four PKD families...
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