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The European Journal of Neuroscience|November 23, 2020
Mutation analysis of MFSD8 in an amyotrophic lateral sclerosis cohort from mainland ChinaLing Huang, Zhen Liu, Yanchun Yuan, et al.
Journal of Neurology|September 1, 2019
Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland ChinaYao Zhou, Yanchun Yuan, Zhen Liu, et al.
Frontiers in Neurology|July 7, 2020
Association Between Vitamins and Amyotrophic Lateral Sclerosis: A Center-Based Survey in Mainland ChinaMengli Wang, Zhen Liu, Weining Sun, et al.
Parkinsonism & Related Disorders|November 15, 2019
Clinical findings of autosomal-dominant striatal degeneration and PDE8B mutation screening in parkinsonism and related disordersJie Ni, Xiaoping Yi, Zhen Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 14, 2018
[Analysis of spinocerebellar ataxia type 31 related mutations among patients from mainland China]Ke Yang, Sheng Zeng, Zhen Liu, et al.
Frontiers in Aging Neuroscience|February 27, 2023
Genetic and clinical analysis of <i>TP73</i> gene in amyotrophic lateral sclerosis patients from Chinese mainlandXuxiong Tang, Yanchun Yuan, Zhen Liu, et al.
Neurobiology of Aging|October 27, 2019
Mutation analysis of GLT8D1 and ARPP21 genes in amyotrophic lateral sclerosis patients from mainland ChinaWanzhen Li, Zhen Liu, Weining Sun, et al.
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