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	GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder.
	Hong Xia; Xiangjun Huang; Hongbo Xu; Yong-An Zhou; Lina Gong; Zhijian Yang; Jingyan Lv; Hao Deng
刊名	Genetics and molecular biology
	2019
卷号	Vol.42 No.1页码:48-51
ISSN号	1415-4757
URL标识	查看原文
公开日期	[db:dc_date_available]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4734566
专题	湖南大学
作者单位	Third Xiangya Hospital, Center for Experimental Medicine and Department of Neurology, Central South University, Changsha, Hunan, China. First Affiliated Hospital, Department of General Surgery, Hunan University, Changsha, Hunan, China. Second Affiliated Hospital, Department of Blood Transfusion, Shaanxi Normal University, Taiyuan, Shanxi, China.
推荐引用方式 GB/T 7714	Hong Xia,Xiangjun Huang,Hongbo Xu,et al. GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder.[J]. Genetics and molecular biology,2019,Vol.42 No.1:48-51.
APA	Hong Xia.,Xiangjun Huang.,Hongbo Xu.,Yong-An Zhou.,Lina Gong.,...&Hao Deng.(2019).GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder..Genetics and molecular biology,Vol.42 No.1,48-51.
MLA	Hong Xia,et al."GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder.".Genetics and molecular biology Vol.42 No.1(2019):48-51.

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