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	Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family
	Wang, Honghan; Wang, Xinwei; He, Chufeng; Li, Haibo; Qing, Jie; Grati, M'hamed; Hu, Zhengmao; Li, Jiada; Hu, Yiqiao; Xia, Kun
刊名	Journal of Human Genetics
	2015
卷号	60期号:3页码:119-126
ISSN号	1434-5161
DOI	10.1038/jhg.2014.114
URL标识	查看原文
WOS记录号	WOS:000351761200003
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3342345
专题	中南大学
作者单位	1.[Mei, Lingyun 2.Feng, Yong 3.Chen, Hongsheng 4.Wang, Honghan 5.Wang, Xinwei 6.Men, Meichao 7.Jiang, Lu 8.Liu, Yalan 9.He, Chufeng 10.Wang, Xingwei] Cent S Univ, Xiangya Hosp, Dept Otolaryngol, Changsha 410008, Hunan, Peoples R China.
推荐引用方式 GB/T 7714	Wang, Honghan,Wang, Xinwei,He, Chufeng,et al. Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family[J]. Journal of Human Genetics,2015,60(3):119-126.
APA	Wang, Honghan.,Wang, Xinwei.,He, Chufeng.,Li, Haibo.,Qing, Jie.,...&Feng, Yong*.(2015).Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.Journal of Human Genetics,60(3),119-126.
MLA	Wang, Honghan,et al."Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family".Journal of Human Genetics 60.3(2015):119-126.

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