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	Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family A case report
	Feng, Lei; Zhou, Daizhan; Zhang, Zhou; He, Lin; Liu, Yun; Yang, Yabo
刊名	MEDICINE
	2017
卷号	96期号:24
关键词	anisometropia exome sequencing UNC5D
ISSN号	0025-7974
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/3621302
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Feng, Lei,Zhou, Daizhan,Zhang, Zhou,et al. Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family A case report[J]. MEDICINE,2017,96(24).
APA	Feng, Lei,Zhou, Daizhan,Zhang, Zhou,He, Lin,Liu, Yun,&Yang, Yabo.(2017).Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family A case report.MEDICINE,96(24).
MLA	Feng, Lei,et al."Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family A case report".MEDICINE 96.24(2017).

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