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

✍ Scribed by Frederico José Silva Corrêa; Adriano Bueno Tavares; Rinaldo Wellerson Pereira; Mauricio Simões Abrão

No coin nor oath required. For personal study only.

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