Figure 3 of Su, Mol Vis 2012; 18:3057-3063.

Figure 3. Partial sequence of CRYAA at exon1. A: The arrow indicates the mutation spot in sequence of affected individual. B: No base change was found in the sequence of unaffected individual. In panel A, the heterozygous mutation c.161G>C was identified in all the affected participants, but was not found in unaffected family members nor in the 100 unrelated control subjects.