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. Author manuscript; available in PMC: 2012 Sep 27.
Published in final edited form as: Br J Ophthalmol. 2011 Mar 28;95(7):1019–1024. doi: 10.1136/bjo.2010.189076

Figure 1.

Figure 1

Pedigree drawing of family PKRP064 with haplotypes of six adjacent 15q markers and segregation of c.466C/T variation with the disease phenotype. Squares are males, circles are females; filled symbols are affected individuals; a double line between individuals indicates consanguinity and a diagonal line through a symbol is deceased family member. The alleles forming the risk haplotype are shaded black, alleles co-segregating with disease haplotype but not showing homozygosity are shaded grey and alleles not co-segregating with fundus albipunctatus are shown in white.