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Mutation analysis of microRNA-7 gene in Chinese patients with Parkinson's disease
  • 期刊名称：Zhong Nan Da Xue Xue Bao Yi Xue Ban
  • 时间：0
  • 页码：1189-1192
  • 相关项目：SUMO化修饰在SCA3/MJD转录抑制发生机制中的作用研究
作者： Zhang X|Shen L|Jiang H|Pan Q|Xia K|Yan X|Tang B|Guo J|Ai S|Hu Y|Sun Q|Xu Q|Lv Z|Li K|Dong X|
同期刊论文项目
SUMO化修饰在SCA3/MJD转录抑制发生机制中的作用研究
期刊论文 23 会议论文 3
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遗传性痉挛性截瘫患者179例的临床与遗传学特点
Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1
LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's disease
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
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Teaching NeuroImages: Leptomeningeal and pachymeningeal enhancement in a patient with spontaneous CS
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population