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	Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia
	Chen, Jiajun; Sun, Yajuan; Liu, Xiaoyang; Li, Jia
刊名	BMC NEUROLOGY
	2019
卷号	19
关键词	Hereditary ataxia ADCA L-type calcium channel CACNA1C Mutation
ISSN号	1471-2377
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3511749
专题	吉林大学白求恩第三医院
推荐引用方式 GB/T 7714	Chen, Jiajun,Sun, Yajuan,Liu, Xiaoyang,et al. Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia[J]. BMC NEUROLOGY,2019,19.
APA	Chen, Jiajun,Sun, Yajuan,Liu, Xiaoyang,&Li, Jia.(2019).Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia.BMC NEUROLOGY,19.
MLA	Chen, Jiajun,et al."Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia".BMC NEUROLOGY 19(2019).

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