REFERENCES
- Allikmets R, Singh N, Sun H, et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet 1997;15:236–246.
- Burke TR, Rhee DW, Smith RT, et al. Quantification of peripapillary sparing and macular involvement in Stargardt Disease (STGD1). Invest Ophthalmol Vis Sci 2011;52:8006–8015.
- Anastasakis A, Fishman GA, Lindeman M, Genead MA, Zhou W. Infrared scanning laser ophthalmoscope imaging of the macula and its correlation with functional loss and structural changes in patients with Stargardt disease. Retina 2011;31:949–958.
- Smith RT, Gomes NL, Barile G, Busuioc M, Lee N, Laine A. Lipofuscin and autofluorescence metrics in progressive STGD. Invest Ophthalmol Vis Sci 2009;50:3907–3914.
- Spaide RF, Curcio CA. Anatomical correlates to the bands seen in the outer retina by optical coherence tomography: literature review and model. Retina 2011;31:1609–1619.
- Fishman GA, Stone EM, Grover S, Derlacki DJ, Haines HL, Hockey RR. Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene. Arch Ophthalmol 1999;117:504–510.
- Cella W, Greenstein VC, Zernant-Rajang J, et al. G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull’s eye maculopathy. Exp Eye Res 2009;89:16–24.