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	NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve
	Wang, Juan; Abhinav, Pradhan; Xu, Ying-Jia; Li, Ruo-Gu; Zhang, Min; Qiu, Xing-Biao; Di, Ruo-Min; Qiao, Qi; Li, Xiu-Mei; Huang, Ri-Tai
刊名	INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
	2019
卷号	43期号:4
关键词	congenital heart disease bicuspid aortic valve genetics transcription factor nuclear receptor subfamily 2 group F member 2 reporter gene assay
ISSN号	1107-3756
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/3597100
专题	复旦大学上海医学院
推荐引用方式 GB/T 7714	Wang, Juan,Abhinav, Pradhan,Xu, Ying-Jia,et al. NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve[J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,2019,43(4).
APA	Wang, Juan.,Abhinav, Pradhan.,Xu, Ying-Jia.,Li, Ruo-Gu.,Zhang, Min.,...&Yang, Yi-Qing.(2019).NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve.INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,43(4).
MLA	Wang, Juan,et al."NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve".INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 43.4(2019).

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