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A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review 期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 36
作者:  Li, Xinyuan;  Zhou, Chunkui;  Cui, Li;  Zhu, Lijun;  Du, Heqian
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/05
A case of a novel CACNA1G mutation from a Chinese family with SCA42 A case report and literature review 期刊论文
MEDICINE, 2018, 卷号: 97, 期号: 36
作者:  Wang, Chenglin;  Li, Xinyuan;  Zhou, Chunkui;  Cui, Li;  Zhu, Lijun
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/05
Identification of Abnormal 51 CTA/CTG Expansion as Probably the Shortest Pathogenic Allele for Spinocerebellar Ataxia-8 in China 期刊论文
NEUROSCIENCE BULLETIN, 2018, 卷号: Vol.34 No.5, 页码: 859-862
作者:  Wang, Minjin;  Guo, Shuo;  Yao, Wencong;  Wang, Jun;  Tao, Jianxia
收藏  |  浏览/下载:4/0  |  提交时间:2019/02/25
Voxel-based meta-analysis of gray and white matter volume abnormalities in spinocerebellar ataxia type 2 期刊论文
BRAIN AND BEHAVIOR, 2018, 卷号: Vol.8 No.9
作者:  Han, Qing;  Yang, Jing;  Xiong, Hai;  Shang, Huifang
收藏  |  浏览/下载:2/0  |  提交时间:2019/02/28
TGM6 gene mutations in undiagnosed cerebellar ataxia patients 期刊论文
PARKINSONISM & RELATED DISORDERS, 2018, 卷号: Vol.46, 页码: 84-86
作者:  Yang, ZH;  Shi, MM;  Liu, YT;  Wang, YL;  Luo, HY
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/26


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