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	GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder
	Xia, Hong; Huang, Xiangjun; Xu, Hongbo; Zhou, Yong-an; Gong, Lina; Yang, Zhijian; Lv, Jingyan; Deng, Hao*
刊名	Genetics and molecular biology
	2019
卷号	42期号:1页码:48-51
关键词	Auditory neuropathy spectrum disorder Exome sequencing GJB2 c.235delC variant GJB2 gene Hearing loss
ISSN号	1415-4757
DOI	10.1590/1678-4685-gmb-2017-0318
URL标识	查看原文
WOS记录号	WOS:000461467100007
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5707503
专题	湖南中医药大学
作者单位	1.[Lv, Jingyan 2.Xu, Hongbo 3.Deng, Hao 4.Yang, Zhijian 5.Xia, Hong 6.Gong, Lina] Cent S Univ, Xiangya Hosp 3, Ctr Expt Med, 138 Tongzipo Rd, Changsha 410013, Hunan, Peoples R China.
推荐引用方式 GB/T 7714	Xia, Hong,Huang, Xiangjun,Xu, Hongbo,et al. GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder[J]. Genetics and molecular biology,2019,42(1):48-51.
APA	Xia, Hong.,Huang, Xiangjun.,Xu, Hongbo.,Zhou, Yong-an.,Gong, Lina.,...&Deng, Hao*.(2019).GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder.Genetics and molecular biology,42(1),48-51.
MLA	Xia, Hong,et al."GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder".Genetics and molecular biology 42.1(2019):48-51.

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