Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.AuthorsLiu, 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.PublicationGenes, Brain & Behavior, 2013, Vol 12, Issue 2, p234ISSN1601-1848Publication typeArticleDOI10.1111/gbb.12008