Authors: Maugeri, A Klevering, BJ Rohrschneider, K Blankenagel, A Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM

Citation: A. Maugeri et al., Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy, AM J HU GEN, 67(4), 2000, pp. 960-966

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