Figure 1 of Kim, Mol Vis 2011; 17:844-853.


Figure 1. Pedigrees of families in which a rhodopsin mutation was identified. The mutation p.Y178C (B) and the mutation p.P347L (E) were segregated with disease phenotype. The newly identified mutation p.A298D (D) was found in a sporadic patient (II-3). Black and white symbols indicate affected and unaffected individuals, respectively. The mutation is represented by “m”; wild-type alleles are represented by “+”; arrows indicate probands.