OR31-06 Candidate Gene Variants in a Large Cohort of Women with Primary Ovarian Insufficiency

Primary ovarian insufficiency (POI) is highly heritable. The majority of cases have no known cause. We hypothesized that mutations in previously identified genes or genes from the same pathways are the cause of POI in a recessive or dominant manner. Subjects included 294 women diagnosed with POI (am...

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Udgivet i:J Endocr Soc
Main Authors: Gorsi, Bushra, Moriwaki, Mika, Moore, Marvin B, Rajkovic, Aleksandar, Nelson, Lawrence M, Yandell, Mark, Welt, Corrine Kolka
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2020
Fag:
Reproductive Endocrinology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207318/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1419
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