Figure 1 of Gandra, Mol Vis 2008; 14:1105-1113.


Figure 1. Clinical and molecular features of the proband (L2:50) with the p.Gly106Arg mutation. A: Pedigree showing the isolated form of the disease. B: Genomic DNA sequences (reverse) of a part of the RHO gene of L2:50 displaying the p.Gly106Arg mutation (top) and of a normal subject (bottom). The rectangular box shows the position of a heterozygous change at nucleotide 316 (c.316G/A, but the sequence shows the reverse sequence boxed as Y). C: Visual field test reveals a sectoral form of RP. D: Fundus (right eye) photograph showing mild retinitis pigmentosa changes.