Fig. 3From: Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome familyProtein structure of the wild-type and the variant c.672_701dup in FOXL2. a wild-type, the red region corresponds to the mutated region in (b); b c.672_701dup, the red region refers to the structural alteration of the mutated regionBack to article page