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	Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China
	Luo, Jianfen; Bai, Xiaohui; Zhang, Fengguo; Xiao, Yun; Gu, Lintao; Han, Yuechen; Fan, Zhaomin; Li, Jianfeng; Xu, Lei; Wang, Haibo
刊名	ANNALS OF HUMAN GENETICS
	2017
卷号	81期号:6页码:258-266
关键词	China GJB2 mutation screening nonsyndromic sensorineural hearing loss profound SLC26A4
DOI	10.1111/ahg.12207
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/4589545
专题	山东大学
作者单位	Shandong Univ, Sha
推荐引用方式 GB/T 7714	Luo, Jianfen,Bai, Xiaohui,Zhang, Fengguo,et al. Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China[J]. ANNALS OF HUMAN GENETICS,2017,81(6):258-266.
APA	Luo, Jianfen.,Bai, Xiaohui.,Zhang, Fengguo.,Xiao, Yun.,Gu, Lintao.,...&Wang, Haibo.(2017).Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.ANNALS OF HUMAN GENETICS,81(6),258-266.
MLA	Luo, Jianfen,et al."Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China".ANNALS OF HUMAN GENETICS 81.6(2017):258-266.

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