脊髓小脑共济失调
遗传学
等位基因
基因
生物
共济失调
马查多-约瑟夫病
疾病
内科学
医学
神经科学
作者
Li Yu,Zhen Liu,Xiaorong Hou,Zhao Chen,Lu Shen,Kun Xia,Beisha Tang,Hong Jiang,Junling Wang
出处
期刊:PubMed
日期:2021-08-28
卷期号:46 (8): 793-799
被引量:4
标识
DOI:10.11817/j.issn.1672-7347.2021.210230
摘要
The CAG repeat in ATXN2 is a major genetic factor for the AAO of patients with SCA2 in China. The CAG repeat length in ATXN3, CACNA1A, ATXN7, TBP, and RAI1 genes might be a potential factor associated with the AAO of SCA2. The CAG repeat in ATXN7 might be a potential factor affecting the Parkinson's syndrome in SCA2.
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