Fragile X Associated Primary Ovarian Insufficiency (FXPOI): Case Report and Literature Review

Abnormalities in the X-linked FMR1 gene are associated with a constellation of disorders, which have broad and profound implications for the person first diagnosed, and extended family members of all ages. The rare and pleiotropic nature of the associated disorders, both common and not, place great...

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Detalles Bibliográficos
Autores principales: Fink, Dorothy A., Nelson, Lawrence M., Pyeritz, Reed, Johnson, Josh, Sherman, Stephanie L., Cohen, Yoram, Elizur, Shai E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278244/
https://www.ncbi.nlm.nih.gov/pubmed/30542367
http://dx.doi.org/10.3389/fgene.2018.00529

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278244/
https://www.ncbi.nlm.nih.gov/pubmed/30542367
http://dx.doi.org/10.3389/fgene.2018.00529

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