The 2588G→C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease - Maugeri, Alessandra; Driel, Marc A. van; Pol, Dorien J. R. van de; Klevering, B. Jeroen; Haren, Frank J. J. van; Tijmes, Nel; Bergen, Arthur A. B.; Rohrschneider, Klaus; Blankenagel, Anita; Pinckers, Alfred J. L. G.; Dahl, Niklas; Brunner, Han G.; et al. (The American journal of human genetics, 1999)
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