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9. ATP-binding cassette subfamily A, member 4 intronic variants c.4773+3A>G and c.5461-10T>C cause Stargardt disease due to defective splicing. Jonsson F; Westin IM; Österman L; Sandgren O; Burstedt M; Holmberg M; Golovleva I Acta Ophthalmol; 2018 Nov; 96(7):737-743. PubMed ID: 29461686 [TBL] [Abstract][Full Text] [Related]
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11. Clinical and molecular characteristics of childhood-onset Stargardt disease. Fujinami K; Zernant J; Chana RK; Wright GA; Tsunoda K; Ozawa Y; Tsubota K; Robson AG; Holder GE; Allikmets R; Michaelides M; Moore AT Ophthalmology; 2015 Feb; 122(2):326-34. PubMed ID: 25312043 [TBL] [Abstract][Full Text] [Related]
12. Novel mutations in CRB1 and ABCA4 genes cause Leber congenital amaurosis and Stargardt disease in a Swedish family. Jonsson F; Burstedt MS; Sandgren O; Norberg A; Golovleva I Eur J Hum Genet; 2013 Nov; 21(11):1266-71. PubMed ID: 23443024 [TBL] [Abstract][Full Text] [Related]
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15. Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa. Klevering BJ; Maugeri A; Wagner A; Go SL; Vink C; Cremers FP; Hoyng CB Ophthalmology; 2004 Mar; 111(3):546-53. PubMed ID: 15019334 [TBL] [Abstract][Full Text] [Related]
16. ABCA4 gene mutations in Japanese patients with Stargardt disease and retinitis pigmentosa. Fukui T; Yamamoto S; Nakano K; Tsujikawa M; Morimura H; Nishida K; Ohguro N; Fujikado T; Irifune M; Kuniyoshi K; Okada AA; Hirakata A; Miyake Y; Tano Y Invest Ophthalmol Vis Sci; 2002 Sep; 43(9):2819-24. PubMed ID: 12202497 [TBL] [Abstract][Full Text] [Related]
17. Fine central macular dots associated with childhood-onset Stargardt Disease. Fujinami K; Singh R; Carroll J; Zernant J; Allikmets R; Michaelides M; Moore AT Acta Ophthalmol; 2014 Mar; 92(2):e157-9. PubMed ID: 24020726 [No Abstract] [Full Text] [Related]
18. Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindness. Huynh N; Jeffrey BG; Turriff A; Sieving PA; Cukras CA Ophthalmic Genet; 2014 Mar; 35(1):51-6. PubMed ID: 24397708 [TBL] [Abstract][Full Text] [Related]