QQ客服 官方微博 反馈留言

	Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alstrom syndrome
	Yang, Lin; Li, Zixiu; Mei, Mei; Fan, Xiaomei; Zhan, Guodong; Wang, Huijun; Huang, Guoying; Wang, Mingbang; Tian, Weidong; Zhou, Wenhao
刊名	BMC MEDICAL GENETICS
	2017
卷号	18
关键词	Alstrom syndrome Whole genome sequencing ALMS1 gene Cone-rod dystrophy
ISSN号	1471-2350
URL标识	查看原文
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3622252
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Yang, Lin,Li, Zixiu,Mei, Mei,et al. Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alstrom syndrome[J]. BMC MEDICAL GENETICS,2017,18.
APA	Yang, Lin.,Li, Zixiu.,Mei, Mei.,Fan, Xiaomei.,Zhan, Guodong.,...&Zhou, Wenhao.(2017).Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alstrom syndrome.BMC MEDICAL GENETICS,18.
MLA	Yang, Lin,et al."Whole genome sequencing identifies a novel ALMS1 gene mutation in two Chinese siblings with Alstrom syndrome".BMC MEDICAL GENETICS 18(2017).

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。