Figure 3 of Minear, Mol Vis 2013; 19:2508-2516.


Figure 3. Variants in the zinc finger E-box binding homeobox 1 (ZEB1, also known as TCF8) gene on chromosome 10p11.22 that have been detected in patients with Fuchs endothelial corneal dystrophy (FECD). The gene is drawn from 5′ to 3′ reflecting its physical orientation on the forward strand of the reference genome. Drawn as described in the caption for Figure 1, with the red font indicating variants identified in our African American FECD cases and variants marked with an asterisk (*) indicating newly identified variants in African Americans with FECD that have not been previously reported in patients with FECD.