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Figure 1 | BMC Medical Genetics

Figure 1

From: Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa

Figure 1

Pedigree structure and haplotype analysis at the RP25 locus. Blackened bars indicate the disease haplotype. Filled squares or filled circles represent male or female individuals affected with RP, respectively. Arrow points to the proband (II2). All patients in the arRP family carry the homozygous haplotype between single nucleotide polymorphisms rs4710292 and rs4710437. The genomic positions of two markers are from Human (Homo sapiens) Genome Browser Gateway, the GRCh37 build version, and six SNPs are from NCBI B37.1 assembly.

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BMC Medical Genetics

ISSN: 1471-2350

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