1. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes. (21st December 2012) Authors: Liu, X.‐R.; Wu, M.; He, N.; Meng, H.; Wen, L.; Wang, J.‐L.; Zhang, M.‐P.; Li, W.‐B.; Mao, X.; Qin, J.‐M.; Li, B.‐M.; Tang, B.; Deng, Y.‐H.; Shi, Y.‐W.; Su, T.; Yi, Y.‐H.; Tang, B.‐S.; Liao, W.‐P. Journal: Genes, brain, and behavior Issue: Volume 12:Number 2(2013:Mar.) Page Start: 234 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes. (21st December 2012) Authors: Liu, X.‐R.; Wu, M.; He, N.; Meng, H.; Wen, L.; Wang, J.‐L.; Zhang, M.‐P.; Li, W.‐B.; Mao, X.; Qin, J.‐M.; Li, B.‐M.; Tang, B.; Deng, Y.‐H.; Shi, Y.‐W.; Su, T.; Yi, Y.‐H.; Tang, B.‐S.; Liao, W.‐P. Journal: Genes, brain, and behavior Issue: Volume 12:Number 2(2013:Mar.) Page Start: 234 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗