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	A novel NHS mutation in a Chinese family with Nance-Horan Syndrome
	Wei, Meirong; Qi, Anhui; Mo, Haiming; Wu, Kailin; Ma, Xu; Wang, Binbin
	2019
卷号	19期号:5页码:4419-4424
关键词	Nance-Horan syndrome NHS actin remodeling regulator congenital cataracts whole exome sequencing co-segregation analysis
ISSN号	1791-2997
DOI	10.3892/mmr.2019.10106
URL标识	查看原文
收录类别	SCIE ; PUBMED
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6343252
专题	中国医学科学院 北京协和医学院
推荐引用方式 GB/T 7714	Wei, Meirong,Qi, Anhui,Mo, Haiming,et al. A novel NHS mutation in a Chinese family with Nance-Horan Syndrome[J],2019,19(5):4419-4424.
APA	Wei, Meirong,Qi, Anhui,Mo, Haiming,Wu, Kailin,Ma, Xu,&Wang, Binbin.(2019).A novel NHS mutation in a Chinese family with Nance-Horan Syndrome.,19(5),4419-4424.
MLA	Wei, Meirong,et al."A novel NHS mutation in a Chinese family with Nance-Horan Syndrome".19.5(2019):4419-4424.

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