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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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Fink, Dorothy A., Nelson, Lawrence M., Pyeritz, Reed, Johnson, Josh, Sherman, Stephanie L., Cohen, Yoram, Elizur, Shai E.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6278244/
https://ncbi.nlm.nih.gov/pubmed/30542367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00529
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