Figure 1 of
Sullivan, Mol Vis 2007;
Figure 1. Pedigree of a large family with Meesmann's corneal dystrophy showing a typical autosomal dominant mode of inheritance
Squares represent males and circles represent females. Filled symbols mark affected individuals. Individuals who contributed DNA samples and were tested for the R430P mutation are marked with a plus sign. Asterisks denote participants who were clinically examined by the authors. Arrow indicates the proband.