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Article

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

Fertility and sterility - 30 Jun 2011

Ojeda Diego, Lakhal Besma, Fonseca Dora Janneth, Braham Rim, Landolsi Hanène, Mateus Heidi Eliana, Restrepo Carlos Martín, Elghezal Hatem, Saâd Ali, Laissue Paul

Abstract excerpt

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.

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Identifiers

PMID: 21575944
DOI: 10.1016/j.fertnstert.2011.04.045

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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