Research Article
Choroidal Thickness Analysis in Patients with Usher Syndrome Type 2 Using EDI OCT
Table 1
USH2A gene mutations in our Usher patients cohort.
| | Patient | Mutation | | Genotype |
| | 1 | c.10450C>T | c.2276G>T | Heterozygous | | 2 | c.5776+1G>C | | Homozygous | | 3 | c.1663C>G | c.2276G>T | Heterozygous | | 4 | c.2276G>T | c.1663C>G | Heterozygous | | 5 | c.1434G>C | c.4106C>T | Heterozygous | | 6 | c.2898delG | | Homozygous | | 7 | c.11864G>A | c.4714C>T | Heterozygous | | 8 | c.2299delG | c.1606T>C | Heterozygous | | 9 | c.1751G>T | c.2276G>T | Heterozygous | | 10 | c.2299delG | c.14074G>A | Heterozygous |
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