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	A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I
	Ma, Jing; Lin, Ken; Jiang, Hong-chao; Yang, Yanli; Zhang, Yu; Yang, Guilian; Sun, Hao; Ming, Cheng; Bi, Xianyun; Zhang, Tiesong
	2019
卷号	7期号:7页码:e798
关键词	gene mutation hereditary deafness PAX3 Waardenburg syndrome type I
ISSN号	2324-9269
DOI	10.1002/mgg3.798
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/6340539
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,Lin, Ken,Jiang, Hong-chao,et al. A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I[J],2019,7(7):e798.
APA	Ma, Jing.,Lin, Ken.,Jiang, Hong-chao.,Yang, Yanli.,Zhang, Yu.,...&Ruan, Biao.(2019).A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I.,7(7),e798.
MLA	Ma, Jing,et al."A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I".7.7(2019):e798.

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