Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations

Figure 3

A pedigree of adRP with the novel RP11  mutation. A family carrying a novel c.613_615delTAC mutation in RP11 is presented. All of 6 family members who underwent molecular diagnosis carried the heterozygous c.613_615delTAC mutation as indicated with [M];[]. Affected individuals are indicated as filled symbols, and an arrow indicates the proband in this family.