Figure 1 of Jonsson, Mol Vis 2018; 24:667-678.

Figure 1. A pedigree chart of a family from northern Sweden. Two siblings affected with severe retinitis pigmentosa were compound heterozygotes for the 91 kb deletion (c.-8162_1145–1212del, p.?) and the missense variant (c.2309A>G, p.Glu770Gly) in the MERTK gene. Shaded symbols indicate affected retinitis pigmentosa (RP) cases. Open symbols represent unaffected family members.