A functional variant in the CFI gene confers a high risk of age-related macular degeneration von van de Ven, Johannes P H, Nilsson, Sara C, Tan, Perciliz L, Buitendijk, Gabriëlle H S, Ristau, Tina, Mohlin, Frida C, Nabuurs, Sander B, Schoenmaker-Koller, Frederieke E, Smailhodzic, Dzenita, Campochiaro, Peter A, Zack, Donald J, Duvvari, Maheswara R, Bakker, Bjorn, Paun, Codrut C, Boon, Camiel J F, Uitterlinden, Andre G, Liakopoulos, Sandra, Klevering, B Jeroen, Fauser, Sascha, Daha, Mohamed R, Katsanis, Nicholas, Klaver, Caroline C W, Blom, Anna M, Hoyng, Carel B, den Hollander, Anneke I

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Analysis of rare variants in the C3 gene in patients with age-related macular degeneration von Duvvari, Maheswara R, Paun, Codrut C, Buitendijk, Gabriëlle H S, Saksens, Nicole T M, Volokhina, Elena B, Ristau, Tina, Schoenmaker-Koller, Frederieke E, van de Ven, Johannes P H, Groenewoud, Joannes M M, van den Heuvel, Lambertus P W J, Hofman, Albert, Fauser, Sascha, Uitterlinden, André G, Klaver, Caroline C W, Hoyng, Carel B, de Jong, Eiko K, den Hollander, Anneke I

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High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population von Collin, Rob W J, van den Born, L Ingeborgh, Klevering, B Jeroen, de Castro-Miró, Marta, Littink, Karin W, Arimadyo, Kentar, Azam, Maleeha, Yazar, Volkan, Zonneveld, Marijke N, Paun, Codrut C, Siemiatkowska, Anna M, Strom, Tim M, Hehir-Kwa, Jayne Y, Kroes, Hester Y, de Faber, Jan-Tjeerd H N, van Schooneveld, Mary J, Heckenlively, John R, Hoyng, Carel B, den Hollander, Anneke I, Cremers, Frans P M

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A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusen von Paun, Codrut C, Pijl, Benjamin J, Siemiatkowska, Anna M, Collin, Rob W J, Cremers, Frans P M, Hoyng, Carel B, den Hollander, Anneke I

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