Figure 1From: Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India Sequence chromatograms of the FECD patients showing the variants along with the controls. a, b. Novel variants identified in the COL8A2 gene. c, d. Novel variants identified in SLC4A11 gene. The underline marks the mutated codon. The arrow indicates heterozygous state of the sequence.Back to article page