Search Results - Tijmes, Nel

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 Starga... by Maugeri, Alessandra (Author) , Driel, Marc A. van (Author) , Pol, Dorien J. R. van de (Author) , Klevering, B. Jeroen (Author) , Haren, Frank J. J. van (Author) , Tijmes, Nel (Author) , Bergen, Arthur A. B. (Author) , Rohrschneider, Klaus (Author) , Blankenagel, Anita (Author) , Pinckers, Alfred J. L. G. (Author) , Dahl, Niklas (Author) , Brunner, Han G. (Author) , Deutman, August F. (Author) , Hoyng, Carel B. (Author) , Cremers, Frans P. M. (Author) ,

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

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