Fig. 1From: Functional study on new FOXL2 mutations found in Chinese patients with blepharophimosis, ptosis, epicanthus inversus syndromeDetection of FOXL2 mutation in BPES patients. a. The Pedigree of a Chinese family with BPES. b. Representative images of BPES patients. c. Sequencing result indicating the c.931C > T mutation in the FOXL2 gene. d. Alignment of FOXL2 proteins from different species showing the conserved site of H311Back to article page