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Unilateral macular oedema in Zermatt and Stargardt macular dystrophiesABOUZEID, H; WOLFENSBERGER, T. J; SCHORDERET, D. F et al.British journal of ophthalmology. 2009, Vol 93, Num 10, issn 0007-1161, 1376-1377, 1407-1408 [4 p.]Article

Clinical and Genetic Characteristics of Late-onset Stargardt's DiseaseHAAFTEN, Sarah C. Westeneng-Van; BOON, Camiel J. F; CREMERS, Frans P. M et al.Ophthalmology (Rochester, MN). 2012, Vol 119, Num 6, pp 1199-1210, issn 0161-6420, 12 p.Article

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Characteristics and low vision corrections in Stargardt's disease: educational and vocational achievements enhanced by low vision correctionsFONDA, G; GARDNER, L. R.Ophthalmology (Rochester, MN). 1985, Vol 92, Num 8, pp 1084-1091, issn 0161-6420Conference Paper

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Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosaKLEVERING, B. Jeroen; MAUGERI, Alessandra; WANNER, Anja et al.Ophthalmology (Rochester, MN). 2004, Vol 111, Num 3, pp 546-553, issn 0161-6420, 8 p.Article

L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatusSCHOLL, Hendrik P. N; KREMERS, Jan; VONTHEIN, Reinhard et al.Investigative ophthalmology & visual science. 2001, Vol 42, Num 6, pp 1380-1389, issn 0146-0404Article

Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4)YATSENKO, Alexander N; SHROYER, Noah F; LEWIS, Richard Alan et al.Human genetics. 2001, Vol 108, Num 4, pp 346-355, issn 0340-6717Article

Complex inheritance of ABCR mutations in Stargardt disease : linkage disequilibrium, complex alleles, and pseudodominanceSHROYER, N. F; LEWIS, R. A; LUPSKI, J. R et al.Human genetics. 2000, Vol 106, Num 2, pp 244-248, issn 0340-6717Article