Figure 1. The pedigrees of the four
Chinese families with autosomal recessive retinitis pigmentosa (arRP)
or Usher syndrome type II (USH2), and with mutations in the USH2A
gene. Pedigree and haplotyping analyses of family one (FR1) showed
segregation with six microsatellite markers on chromosome 1 listed in
descending order from the centromeric end. Squares indicate males;
circles indicate females; slashed symbols indicate deceased; solid
symbols indicate affected; open symbols indicate unaffected; and arrow
symbol indicates proband. The genotype of each evaluated individual is
shown below the individual’s symbol and identification number.
Abbreviations: Wild type (W); p.C934W (M1); p. W2744C (M2); p. R626X
(M3); p. I2084fs (M4); p. W1263X (M5); p. D3165fs(M6); p.G2375fs (M7);
p.Y4801X (M8).