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Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome

Crossref DOI link: https://doi.org/10.1007/s10815-020-01931-2

Published Online: 2020-08-28

Published Print: 2020-11

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

Authors

Zhang, Zhihua

Wu, Ling

Diao, Feiyang

Chen, Biaobang

Fu, Jing

Mao, Xiaoyan

Yan, Zheng

Li, Bin

Mu, Jian

Zhou, Zhou

Wang, Wenjing

Zhao, Lin

Dong, Jie

Zeng, Yang

Du, Jing

Kuang, Yanping

Sun, Xiaoxi

He, Lin

Sang, Qing https://orcid.org/0000-0002-9895-1394
Wang, Lei
Funding

Funding for this research was provided by:

National Basic Research Program of China (2018YFC1003800, 2017YFC1001500, and 2016YFC1000600)

Natural Science Foundation of Shanghai (19ZR1444500, 17ZR1401900)

The Strategic Collaborative Research Program of the Ferring Institute of Reproductive Medicine, Ferring Pharmaceuticals and Chinese Academy of Sciences (FIRMC200507)

China Postdoctoral Science Foundation (2019M660093)
License Information

Text and Data Mining valid from 2020-08-28

Version of Record valid from 2020-08-28
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Article History

Received: 8 April 2020

Accepted: 18 August 2020

First Online: 28 August 2020

Compliance with ethical standards

:

: The authors declare that they have no conflict of interest.

: All studies on human subjects were approved by the ethics committee of the Medical College of Fudan University.

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