References (cont’d)

  1. Johnson S, Michaelides M, Aligianis IA et al. Achromatopsia caused by novel mutations in both CNGA3 and CNGB3. J Med Genet 2004; 41: e20
  2. Barthelmes D, Sutter FK, Kurz-Levin MM et al. Quantitative Analysis of OCT Characteristics in Patients with Achromatopsia and Blue-Cone Monochromatism. Invest Ophthalmol Vis Sci 2006; 47: 1161-1166
  3. Ozdek S, Onaran Z, Gurelik G, Bilgihan K, Ascar C, Hasanreisoglu B. Stargardt’s disease and retinitis pigmentosa: different phenotypic presentations in the same family. Eye 2005; 19: 1222-1225
  4. Wada Y, Abe T, Fuse N, Tamaj M. A Frequent 1085delC/InsGAAG Mutation in the RDH5 Gene in Japanese Patients with Fundus Albipunctatus. Invest Ophthalmol Vis Sci 2000; 41: 1894-1897
  5. Tomohiro 0, Yumika Y, Shoji K. Correlation Between Visual Acuity and Foveal Microstructural Changes in Diabetic Macular Edema. Retina 2010; 30(5): 774-780.
  6. Sherman J, Yannuzzi LA, Madonna RJ, Nath S, Bababekova Y. Photoreceptor Integrity Line As Revealed By Spectral Domain OCT. 2009