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Neuroscience Letters|July 31, 2013
Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseasesJun-Ling Wang, Xiao Mao, Zheng-Mao Hu, et al.Neurobiology of Aging|June 4, 2013
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disordersZhao Chen, Jun-Ling Wang, Bei-Sha Tang, et al.Cerebellum (London, England)|July 15, 2021
Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First TimeYue Xie, Zhao Chen, Zhe Long, et al.Brain : a Journal of Neurology|November 29, 2011
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesiasJun-Ling Wang, Li Cao, Xun-Hua Li, et al.Pageof 3