Figure 5
From: Identifying mutations in Tunisian families with retinal dystrophy
Overview of the pedigree structure of the families and segregation analysis of disease causing variants in the RD cohort.
Arrows point to the probands. Affected individuals are indicated with filled symbols (blue), suspected (grey), whereas unaffected relatives are indicated by open symbols. +: wild type allele; −: mutation. All mutations are homozygous except for family F7.Genes with new mutations are in bold.
