Fig. 1
From: A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa
Pedigree, LRAT Region, and sequence. a Haplotypes of the LRAT region of family 61254 showing the LRAT c.541-15T>G mutation and surrounding microsatellite markers included in Table 1. The risk haplotype is marked in black. b Electropherograms of the LRAT homozygous mutation c.541-15T>G (up, individual 7), carrier sequence (middle, individual 22), and wildtype alleles (down, individual 41)