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Article

FOXL2: a gene central to ovarian function.

Journal of clinical pathology - 1 Dec 2023

Mubeen Aysha, Parra-Herran Carlos

Abstract excerpt

The FOXL2 (forkhead box L2) gene is located on chromosome 3 and encodes for forkhead box (FOX) family of transcription factors which play a critical role in various biological processes. Germline FOXL2 mutations have been identified in blepharophimosis/ptosis/epicanthus inversus syndrome. The somatic missense mutation in FOXL2 (FOXL2 C134W) is now known to be the defining molecular feature of adult-type granulosa...

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Identifiers

PMID: 37798106
DOI: 10.1136/jcp-2023-208827

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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