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2. New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease. Simonelli F, Testa F, de Crecchio G, Rinaldi E, Hutchinson A, Atkinson A, Dean M, D'Urso M, Allikmets R. Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):892-7. PubMed ID: 10711710 [Abstract] [Full Text] [Related]
11. Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease. Lewis RA, Shroyer NF, Singh N, Allikmets R, Hutchinson A, Li Y, Lupski JR, Leppert M, Dean M. Am J Hum Genet; 1999 Feb; 64(2):422-34. PubMed ID: 9973280 [Abstract] [Full Text] [Related]
14. Molecular genetic analysis of ABCR gene in Japanese dry form age-related macular degeneration. Fuse N, Suzuki T, Wada Y, Yoshida M, Shimura M, Abe T, Nakazawa M, Tamai M. Jpn J Ophthalmol; 2000 Feb; 44(3):245-9. PubMed ID: 10913642 [Abstract] [Full Text] [Related]
18. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, Peiffer A, Zabriskie NA, Li Y, Hutchinson A, Dean M, Lupski JR, Leppert M. Science; 1997 Sep 19; 277(5333):1805-7. PubMed ID: 9295268 [Abstract] [Full Text] [Related]
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