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...
Autores Principales: | , , , , , , , , |
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Formato: | Artículo (Article) |
Lenguaje: | Inglés (English) |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://repository.urosario.edu.co/handle/10336/22923 https://doi.org/10.1016/j.rbmo.2011.11.017 |