Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa

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Figure 1  .

SSCP analysis and pedigree of the family. To detect point mutations, the entire rhodopsin coding sequence, including the five exons and their exon-intron junctions, was amplified using a "multiplex-PCR".³ Shaded symbols represent those affected.

Figure 2  .

Fluorescein angiogram of patient II-1.