Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR - Cremers, Frans; van de Pol, Dorien J. R.; van Driel, Marc; den Hollander, Anneke I.; van Haren, Frank J. J.; Knoers, Nine V. A. M.; Tijmes, Nel; Bergen, Arthur A. B.; Rohrschneider, Klaus; Blankenagel, Anita; Pinckers, Alfred Joseph Lambert Gérard; Deutman, August F.; et al. (Human molecular genetics, 1998)
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