Figure 1.

In PKRP063, haplotypes of 6p markers and segregation of c.1138A>G variation with the disease phenotype. A square represents a male individual; a circle, a female individual; shading, an affected individual; a double line, consanguinity; and a slash mark, a deceased individual. Haplotypes with alleles forming the risk haplotype are shaded black, and alleles not cosegregating with autosomal recessive retinitis pigmentosa are white.