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	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:329
关键词	hereditary inclusion body myopathy next-generation sequencing CFTR mutation whole-exome sequencing
ISSN号	1662-453X
DOI	10.3389/fnins.2018.00329
URL标识	查看原文
收录类别	SCIE ; PUBMED
WOS记录号	WOS:000432696300001
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5932920
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. Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis[J]. FRONTIERS IN NEUROSCIENCE,2018,12:329.
APA	Lu, Yan.,Da, Yu-Wei.,Zhang, Yong-Biao.,Li, Xin-Gang.,Wang, Min.,...&Lei, Lin.(2018).Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis.FRONTIERS IN NEUROSCIENCE,12,329.
MLA	Lu, Yan,et al."Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis".FRONTIERS IN NEUROSCIENCE 12(2018):329.

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