Publication Details

AFRICAN RESEARCH NEXUS

SHINING A SPOTLIGHT ON AFRICAN RESEARCH

medicine

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

Fertility and Sterility, Volume 95, No. 8, Year 2011

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.
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Citations: 17
Authors: 10
Affiliations: 2
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Research Areas
Cancer
Genetics And Genomics
Health System And Policy
Maternal And Child Health
Sexual And Reproductive Health