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	Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99
	Li, Jiangxia; Zhao, Xiaohan; Xin, Qian; Shan, Shan; Jiang, Baichun; Jin, Yecheng; Yuan, Huijun; Dai, Pu; Xiao, Ruo; Zhang, Qingyan
刊名	Human mutation
	2015
卷号	36期号:1页码:98-105
关键词	ARNSHL DFNB99 TMEM132E inner hair cell whole-exome sequencing
DOI	10.1002/humu.22712
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4793424
专题	山东大学
作者单位	Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, Shandong University School of Medicin
推荐引用方式 GB/T 7714	Li, Jiangxia,Zhao, Xiaohan,Xin, Qian,et al. Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99[J]. Human mutation,2015,36(1):98-105.
APA	Li, Jiangxia.,Zhao, Xiaohan.,Xin, Qian.,Shan, Shan.,Jiang, Baichun.,...&Xiao.(2015).Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.Human mutation,36(1),98-105.
MLA	Li, Jiangxia,et al."Whole-Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99".Human mutation 36.1(2015):98-105.

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