1. Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. (27th December 2017) Authors: Yin, Xiao-Meng; Lin, Jing-Han; Cao, Li; Zhang, Tong-Mei; Zeng, Sheng; Zhang, Kai-Lin; Tian, Wo-Tu; Hu, Zheng-Mao; Li, Nan; Wang, Jun-Ling; Guo, Ji-Feng; Wang, Ruo-Xi; Xia, Kun; Zhang, Zhuo-Hua; Yin, Fei; Peng, Jing; Liao, Wei-Ping; Yi, Yong-Hong; Liu, Jing-Yu; Yang, Zhi-Xian Journal: Human molecular genetics Issue: Volume 27:Number 4(2018:Feb. 15) Page Start: 625 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. (16th January 2018) Authors: Yin, Xiao-Meng; Lin, Jing-Han; Cao, Li; Zhang, Tong-Mei; Zeng, Sheng; Zhang, Kai-Lin; Tian, Wo-Tu; Hu, Zheng-Mao; Li, Nan; Wang, Jun-Ling; Guo, Ji-Feng; Wang, Ruo-Xi; Xia, Kun; Zhang, Zhuo-Hua; Yin, Fei; Peng, Jing; Liao, Wei-Ping; Yi, Yong-Hong; Liu, Jing-Yu; Yang, Zhi-Xian Journal: Human molecular genetics Issue: Volume 27:Number 4(2018:Feb. 15) Page Start: 757 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗