CORC  > 中国医学科学院 北京协和医学院
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
2019
卷号19期号:3页码:1775-1780
关键词Waardenburg syndrome type 2 hereditary deafness SRY-box 10 gene gene mutation
ISSN号1791-2997
DOI10.3892/mmr.2019.9815
URL标识查看原文
收录类别SCIE ; PUBMED
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/6345194
专题中国医学科学院 北京协和医学院
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],2019,19(3):1775-1780.
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.,19(3),1775-1780.
MLA Ma, Jing,et al."A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II".19.3(2019):1775-1780.
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