QQ客服 官方微博 反馈留言

	Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
	Lu Yan; Da Yu-Wei; Zhang Yong-Biao; Li Xin-Gang; Wang Min; Di Li; Pang Mi; Lei Lin
刊名	Frontiers in neuroscience
	2018
卷号	12页码:570
关键词	CFTR hereditary inclusion body myopathy mutation next-generation sequencing whole-exome sequencing
ISSN号	1662-4548
DOI	10.3389/fnins.2018.00570
URL标识	查看原文
收录类别	PUBMED
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5930003
专题	北京航空航天大学
推荐引用方式 GB/T 7714	Lu Yan,Da Yu-Wei,Zhang Yong-Biao,et al. Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis[J]. Frontiers in neuroscience,2018,12:570.
APA	Lu Yan.,Da Yu-Wei.,Zhang Yong-Biao.,Li Xin-Gang.,Wang Min.,...&Lei Lin.(2018).Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis.Frontiers in neuroscience,12,570.
MLA	Lu Yan,et al."Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis".Frontiers in neuroscience 12(2018):570.

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。