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Article

The mutations and potential targets of the forkhead transcription factor FOXL2.

Molecular and cellular endocrinology - 30 Jan 2008

Moumné L, Batista F, Benayoun B A, Nallathambi J, Fellous M, Sundaresan P, Veitia R A

Abstract excerpt

Mutations of FOXL2, a gene encoding a forkhead transcription factor, have been shown to cause the blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). This genetic disorder is characterized by eyelid and mild craniofacial abnormalities that can appear associated with premature ovarian failure. FOXL2 is one of the earliest ovarian markers and it offers, along with its targets, an excellent model to study...

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Source

Identifiers

PMID: 18155828
DOI: 10.1016/j.mce.2007.11.006

Genes

FOXL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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