QQ客服 官方微博 反馈留言

	A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401+1G > A) in CLCN1 gene of a Chinese Han patient
	Miao, Jing; Wei, Xiao-jing; Liu, Xue-mei; Kang, Zhi-xia; Gao, Yan-lu; Yu, Xue-fan
刊名	BMC NEUROLOGY
	2018
卷号	18
关键词	Myotonia congenita Autosomal recessive Case report CLCN1 gene
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/3536418
专题	吉林大学白求恩第一医院
推荐引用方式 GB/T 7714	Miao, Jing,Wei, Xiao-jing,Liu, Xue-mei,et al. A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401+1G > A) in CLCN1 gene of a Chinese Han patient[J]. BMC NEUROLOGY,2018,18.
APA	Miao, Jing,Wei, Xiao-jing,Liu, Xue-mei,Kang, Zhi-xia,Gao, Yan-lu,&Yu, Xue-fan.(2018).A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401+1G > A) in CLCN1 gene of a Chinese Han patient.BMC NEUROLOGY,18.
MLA	Miao, Jing,et al."A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401+1G > A) in CLCN1 gene of a Chinese Han patient".BMC NEUROLOGY 18(2018).

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。