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A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

Crossref DOI link: https://doi.org/10.1186/s12967-018-1633-1

Published Online: 2018-09-21

Published Print: 2018-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Hong, Nanchao

Zhang, Erge

Wang, Qingjie

Zhang, Xiaoqing

Li, Fen

Fu, Qihua

Xu, Rang

Yu, Yu

Chen, Sun

Xu, Yuejuan

Sun, Kun
Funding

Funding for this research was provided by:

grant from the National Natural Science Foundation of China (81670285, 81300068, 81771623, 81741066)

grant from Shanghai Municipal Commission of Health and Family Planning (GWIV-23)

grant from Shanghai Hospital Development Center (SHDC12015102)
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Article History

Received: 31 January 2018

Accepted: 16 September 2018

First Online: 21 September 2018

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