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	Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family
	Zheng, Sui-Lian; Zhang, Hong-Liang; Lin, Zhen-Lang; Kang, Qian-Yan
刊名	INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
	2015
卷号	36期号:[db:dc_citation_issue]页码:1035-1041
关键词	USH2A gene mutation whole-exome sequencing Usher syndrome
ISSN号	1107-3756
DOI	[db:dc_identifier_doi]
URL标识	查看原文
WOS记录号	[DB:DC_IDENTIFIER_WOSID]
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3255320
专题	西安交通大学
推荐引用方式 GB/T 7714	Zheng, Sui-Lian,Zhang, Hong-Liang,Lin, Zhen-Lang,et al. Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family[J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,2015,36([db:dc_citation_issue]):1035-1041.
APA	Zheng, Sui-Lian,Zhang, Hong-Liang,Lin, Zhen-Lang,&Kang, Qian-Yan.(2015).Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family.INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,36([db:dc_citation_issue]),1035-1041.
MLA	Zheng, Sui-Lian,et al."Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family".INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 36.[db:dc_citation_issue](2015):1035-1041.

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