2009•Fertility and SterilityOpen access

A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome

Frederico JS Correa, Adriano Bueno Tavares, Rinaldo Wellerson Pereira, Maurício Simões Abrão

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Key concepts: Blepharophimosis, Hypergonadotropic hypogonadism, Ptosis, Premature ovarian failure, Mutation, Genetics, Gene mutation, Medicine

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A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome — Research Paper | ScholarLens