QQ客服 官方微博 反馈留言

	A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II
	Ma, Jing; Zhang, Zhen; Jiang, Hong-Chao; Sun, Hao; Ming, Cheng; Zhao, Li-Ping; Gao, Ying-Qin; Li, Zheng-Cai; Sun, Mei-Hua; Xiao, Yang
刊名	MOLECULAR MEDICINE REPORTS
	2019
卷号	19期号:3
关键词	Waardenburg syndrome type 2 hereditary deafness SRY-box 10 gene gene mutation
ISSN号	1791-2997
语种	英语
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/3412460
专题	昆明医科大学
推荐引用方式 GB/T 7714	Ma, Jing,Zhang, Zhen,Jiang, Hong-Chao,et al. A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II[J]. MOLECULAR MEDICINE REPORTS,2019,19(3).
APA	Ma, Jing.,Zhang, Zhen.,Jiang, Hong-Chao.,Sun, Hao.,Ming, Cheng.,...&Ruan, Biao.(2019).A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II.MOLECULAR MEDICINE REPORTS,19(3).
MLA	Ma, Jing,et al."A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II".MOLECULAR MEDICINE REPORTS 19.3(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。