Screening for mutations of the FOXO4 gene in premature ovarian failure patients

FOXO4 constitutes a coherent candidate gene associated with premature ovarian failure (POF) pathogenesis. This study sequenced the coding and exon-flanking regions of this gene in a panel of 116 POF patients and 143 controls of Tunisian origin. In both groups, the IVS2 + 41T > G sequence variant...

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Detalles Bibliográficos
Autores Principales: Fonseca-Mendoza, Dora Janeth, Restrepo, Carlos M., Laissue, Paul, Garzón, Eliana, Lakhal, Besma, Braham, Rim, Ojeda, Diego, Elghezal, Hatem, Saâd, Ali
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2012
Materias:
dna
Acceso en línea:https://repository.urosario.edu.co/handle/10336/22923
https://doi.org/10.1016/j.rbmo.2011.11.017

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