Rare variants in GPR3 in POI patients: a case series with review of literature

BACKGROUND: Premature ovarian insufficiency (POI) is a highly heterogeneous disease, and up to 25% of the cases can be explained by genetic causes. G protein-coupled receptor 3 (GPR3) plays an important role in oocyte arrest, and Gpr3-deficient mice exhibited POI-like phenotypes. CASE PRESENTATION:...

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Detalles Bibliográficos
Autores principales: Ren, Shuting, Zhang, Feng, Shang, Lingyue, Yang, Xi, Pan, Yuncheng, Zhang, Xiaojin, Wu, Yanhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623876/
https://www.ncbi.nlm.nih.gov/pubmed/37919810
http://dx.doi.org/10.1186/s13048-023-01282-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623876/
https://www.ncbi.nlm.nih.gov/pubmed/37919810
http://dx.doi.org/10.1186/s13048-023-01282-3

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