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Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure.

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology - 1 Apr 2010

Ni Feng, Wen Qiaolian, Wang Binbin, Zhou Sirui, Wang Jing, Mu Yuan, Ma Xu, Cao Yunxia

Abstract excerpt

Premature ovarian failure (POF) has recently been associated with mutations in Forkhead L2 (FOXL2) gene, which also being a candidate for blepharophimosis-ptosis-epicanthus inversus (BPES) syndrome. In the current study, we performed a screening analysis by polymerase chain reaction and direct sequencing in 118 patients, including one with BPES and her family of six members. The results came back with no novel...

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Source

Identifiers

PMID: 20222838
DOI: 10.3109/09513590903225358

Genes

FOXL2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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