Agretti P

ORCID: 0000-0002-3504-5204 · 1 paper in corpus · active 2021
2021
Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI.
Journal of ovarian research ·doi:10.1186/s13048-021-00836-7

BackgroundPremature ovarian insufficiency (POI) is an ovarian defect characterized by primary or secondary amenorrhea, hypergonadotropism and hypoestrogenism which occurs before the age of 40 years with a major genetic component. In this st…