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Citation: Ai. Den Hollander et al., Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12), NAT GENET, 23(2), 1999, pp. 217-221

Authors: den Hollander, AI van Driel, MA de Kok, YJM van de Pol, DJR Hoyng, CB Brunner, HG Deutman, AF Cremers, FPM

Citation: Ai. Den Hollander et al., Isolation and mapping of novel candidate genes for retinal disorders usingsuppression subtractive hybridization, GENOMICS, 58(3), 1999, pp. 240-249

Authors: Klevering, BJ van Driel, M van de Pol, DJR Pinckers, AJLG Cremers, FPM Hoyng, CB

Citation: Bj. Klevering et al., Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene, BR J OPHTH, 83(8), 1999, pp. 914-918

Authors: Maugeri, A van Driel, MA van de Pol, DJR Klevering, BJ van Haren, FJJ Tijmes, N Bergen, AAB Rohrschneider, K Blankenagel, A Pinckers, AJLG Dahl, N Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM

Citation: A. Maugeri et al., The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease, AM J HU GEN, 64(4), 1999, pp. 1024-1035