Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

"Earlier reports demonstrated a key role of Cdkn1b during mouse ovarian development. In this study, the sequencing analysis of the complete coding region of this gene in a panel of premature ovarian failure patients and control subjects reveals a novel mutation potentially related to the phenot...

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Detalles Bibliográficos
Autores Principales: Ojeda D., Lakhal B., Fonseca-Mendoza, Dora Janeth, Braham R., Landolsi H., Mateus H.E., Restrepo C.M., Elghezal H., Saâd A., Laissue P.
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: Elsevier Inc. 2011
Materias:
Acceso en línea:https://repository.urosario.edu.co/handle/10336/24059
https://doi.org/10.1016/j.fertnstert.2011.04.045