Spinocerebellar ataxia 17 (SCA17) is an autosomal dominant neurodegenerative disease clinically characterized by the presence of cerebellar ataxia in combination with variable neurological symptoms. Here we report a Chinese SCA17 family which proband's clinical manifestation was inconsistent with the neuroimage findings.
基金：
Ministry of Health Foundation of China; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC)
第一作者单位：[1]China Japan Friendship Hosp, Movement Disorder & Neurogenet Res Ctr, Beijing 100029, Peoples R China
通讯作者：
通讯机构：[1]China Japan Friendship Hosp, Movement Disorder & Neurogenet Res Ctr, Beijing 100029, Peoples R China[*1]China Japan Friendship Hosp, Movement Disorder & Neurogenet Res Ctr, Yinghua East St, Beijing 100029, Peoples R China
推荐引用方式(GB/T 7714)：
Zhang Jin,Gu Weihong,Hao Ying,et al.Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings[J].ANNALS of INDIAN ACADEMY of NEUROLOGY.2013,16(4):703-704.doi:10.4103/0972-2327.120457.
APA：
Zhang, Jin,Gu, Weihong,Hao, Ying&Chen, Yuanyuan.(2013).Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings.ANNALS of INDIAN ACADEMY of NEUROLOGY,16,(4)
MLA：
Zhang, Jin,et al."Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings".ANNALS of INDIAN ACADEMY of NEUROLOGY 16..4(2013):703-704
