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. 2006 Mar 31;20(1):62–64. doi: 10.3341/kjo.2006.20.1.62

Fig. 4.

Fig. 4

Pedigree of a family, and sequences of regions with mutations in the XLRS1 gene. The blackened symbol denotes phenotypically affected individual. Asterisks(*) denote individuals whose leukocyte DNA was analyzed. Direct sequencing of exon 4. The patient had a missense mutation (Leu103Phe). The altered nucleotides are shown in boldface and are denoted with arrows.