A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B

Epilepsia, EarlyView.

Source: Epilepsia - July 16, 2018 Category: Neurology Authors: Hongying Ma , Shenglei Feng , Xuejun Deng , Li Wang , Sheng Zeng , Cheng Wang , Xixiang Ma , Hao Sun , Rui Chen , Shiyue Du , Jinglin Mao , Xianwei Zhang , Cong Ma , Hong Jiang , Luoying Zhang , Beisha Tang , Jing Yu Liu Source Type: research