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Article

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

JBRA assisted reproduction - 17 Apr 2022

Ramos Cinthia, Ocampos Maristela, Barbato Ingrid Tremel, Niehues Viviane Margareth Scantamburlo, Bicalho Maria da Graça, Nisihara Renato

Abstract excerpt

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 to December 2018 at a University Hospital in Curitiba, Brazil. Genomic DNA was extracted and analyzed using...

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Identifiers

PMID: 34542254
DOI: 10.5935/1518-0557.20210063
PMCID: PMC9118958

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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