QQ客服 官方微博 反馈留言

	A dominant variant in DMXL2 is linked to nonsyndromic hearing loss
	Chai, Yongchuan/37033504500[4]; Chen, Dongye/55891028000[0]; Liu, Xingfeng/57194699190[1]; Lin, Xiaojiang/56656872400[2]; Zhang, Dan/56656676500[3]; Yu, Dehong/56645359200[5]; Sun, Changling/56413354900[6]; Wang, Xueling/56646678200[7]; Zhu, Weidong/56652839800[8]; Chen, Ying/56021300100[9]
刊名	Genetics in Medicine
	2017
卷号	19期号:5
关键词	autosomal dominant DMXL2 inner ear nonsyndromic hearing loss synaptic vesicle
ISSN号	1098-3600
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/3623004
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Chai, Yongchuan/37033504500[4],Chen, Dongye/55891028000[0],Liu, Xingfeng/57194699190[1],et al. A dominant variant in DMXL2 is linked to nonsyndromic hearing loss[J]. Genetics in Medicine,2017,19(5).
APA	Chai, Yongchuan/37033504500[4].,Chen, Dongye/55891028000[0].,Liu, Xingfeng/57194699190[1].,Lin, Xiaojiang/56656872400[2].,Zhang, Dan/56656676500[3].,...&Wu, Hao/56510473500[15].(2017).A dominant variant in DMXL2 is linked to nonsyndromic hearing loss.Genetics in Medicine,19(5).
MLA	Chai, Yongchuan/37033504500[4],et al."A dominant variant in DMXL2 is linked to nonsyndromic hearing loss".Genetics in Medicine 19.5(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。