Association between mutations in the FMR1 gene and ovarian dysfunction in Brazilian patients

OBJECTIVE: Our study aimed to identify mutations in the FMR1 gene in a group of Brazilian women diagnosed with primary ovarian insufficiency (POI). METHODS: This cross-sectional study included patients aged under 40 years with confirmed POI from a convenience sample of patients seen from June 2017 t...

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Detalles Bibliográficos
Autores principales: Ramos, Cinthia, Ocampos, Maristela, Barbato, Ingrid Tremel, Niehues, Viviane Margareth Scantamburlo, Bicalho, Maria da Graça, Nisihara, Renato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Brazilian Society of Assisted Reproduction 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118958/
https://www.ncbi.nlm.nih.gov/pubmed/34542254
http://dx.doi.org/10.5935/1518-0557.20210063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118958/
https://www.ncbi.nlm.nih.gov/pubmed/34542254
http://dx.doi.org/10.5935/1518-0557.20210063

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