Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI)

Fragile X syndrome (FXS) and its associated disorders are caused by the expansion of the CGG repeat in the 5′ untranslated region of the fragile X mental retardation 1 gene (FMR1). The full mutation, defined as >200 cytosine-guanine-guanine (CGG) triplet repeats, causes FXS. Individuals with 55–1...

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Detalles Bibliográficos
Autor principal: Peprah, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141264/
https://www.ncbi.nlm.nih.gov/pubmed/25134882
http://dx.doi.org/10.1186/1742-4755-11-67

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4141264/
https://www.ncbi.nlm.nih.gov/pubmed/25134882
http://dx.doi.org/10.1186/1742-4755-11-67

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