QQ客服 官方微博 反馈留言

	Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families
	Hu, Yan-Shan; Song, Hui; Li, Yin; Xiao, Zi-Yun; Li, Tuo
刊名	INTERNATIONAL JOURNAL OF OPHTHALMOLOGY
	2019
卷号	12期号:6
关键词	retinitis pigmentosa nonsyndromic whole-exome sequencing mutation novel
ISSN号	2222-3959
DOI	10.18240/ijo.2019.06.06
URL标识	查看原文
收录类别	SCIE
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4214902
专题	武汉大学
推荐引用方式 GB/T 7714	Hu, Yan-Shan,Song, Hui,Li, Yin,et al. Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families[J]. INTERNATIONAL JOURNAL OF OPHTHALMOLOGY,2019,12(6).
APA	Hu, Yan-Shan,Song, Hui,Li, Yin,Xiao, Zi-Yun,&Li, Tuo.(2019).Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families.INTERNATIONAL JOURNAL OF OPHTHALMOLOGY,12(6).
MLA	Hu, Yan-Shan,et al."Whole-exome sequencing identifies novel mutations in genes responsible for retinitis pigmentosa in 2 nonconsanguineous Chinese families".INTERNATIONAL JOURNAL OF OPHTHALMOLOGY 12.6(2019).

个性服务

查看访问统计

相关权益政策

暂无数据

收藏/分享

除非特别说明，本系统中所有内容都受版权保护，并保留所有权利。