The association of FMR1 gene (CGG)n variation with idiopathic female infertility

INTRODUCTION: The FMR1 gene plays an important role in brain development and in the regulation of ovarian function. The FMR1 gene contains CGG repeat variation and the expansion of the repeats is associated with various phenotypes e.g. fragile X syndrome, premature ovarian failure, etc. Repeats rang...

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Detalles Bibliográficos
Autores principales: Grasmane, Adele, Rots, Dmitrijs, Vitina, Zane, Magomedova, Valerija, Gailite, Linda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2019
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425234/
https://www.ncbi.nlm.nih.gov/pubmed/34522259
http://dx.doi.org/10.5114/aoms.2019.85154

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8425234/
https://www.ncbi.nlm.nih.gov/pubmed/34522259
http://dx.doi.org/10.5114/aoms.2019.85154

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