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

abstract

  • 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.

publication date

  • 2011/6/30

keywords

  • Genes
  • Mutation
  • Phenotype
  • Primary Ovarian Insufficiency
  • Sequence Analysis

International Standard Serial Number (ISSN)

  • 0015-0282