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Distribution of the likely causative genes in our IRD cohort.
| Clinical diagnosis | Solved cases/Total number of cases | Mutated genes (number of cases) |
|---|---|---|
| ar Retinitis Pigmentosa | 3/4 | USH2A (3) |
| simplex Retinitis Pigmentosa | 8/17 | USH2A (8) |
| Leber congenital amaurosis | 1/1 | LRAT (1) |
| Stargardt disease | 1/3 | ABCA4 (1) |
| Usher Syndrome | 3/3 | USH2A (3) |
| ar Cone dystrophy | 1/1 | CNGB3 (1) |
ar: Autosomal recessive.
