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See Latest ArticlesFOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report
Human Reproduction, 10/13/09
Touraine P et al. – FOXL2 mutations cause the autosomal dominant Blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) that may be associated with premature ovarian failure (POF). However, little is known about the molecular mechanisms of FOXL2 actions in the human ovary.
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