A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency

Article ID	Journal	Published Year	Pages	File Type
8779971	Fertility and Sterility	2017	8 Pages	PDF

Abstract

The mutation p.R59X in FSHR is causative for POI by means of arresting folliculogenesis.

Keywords

mutation ovarian follicle Primary ovarian insufficiency

Related Topics

Health Sciences Medicine and Dentistry Obstetrics, Gynecology and Women's Health

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A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency

Authors

Hongli M.D., Ph.D., Xiaofei M.D., Ph.D., Ting M.D., Ph.D., Lei M.D., Ph.D., Lei M.S., Yingying M.D., Ph.D., Wen M.D., Ph.D., Shidou M.D., Ph.D., Zi-Jiang M.D., Ph.D.,