Abstracto 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 phenotype. © 2011 by American Society for Reproductive Medicine.
autores Ali Saâd Besma Lakhal Diego A. Ojeda Fonseca Mendoza, Dora Janeth Hanène Landolsi Hatem Elghezal Heidi Eliana Mateus Arbelaez Restrepo Fernández, Carlos Martín Rim Braham
