Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration von Yang, Zhenglin, Alvarez, Bernardo V., Chakarova, Christina, Jiang, Li, Karan, Goutam, Frederick, Jeanne M., Zhao, Yu, Sauvé, Yves, Li, Xi, Zrenner, Eberhart, Wissinger, Bernd, Hollander, Anneke I. Den, Katz, Bradley, Baehr, Wolfgang, Cremers, Frans P., Casey, Joseph R., Bhattacharya, Shomi S., Zhang, Kang

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Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4 von Yvette J. M. de Kok, van der Maarel, Silvère M., Bitner-Glindzicz, Maria, Huber, Irene, Monaco, Anthony P., Malcolm, Susan, Pembrey, Marcus E., Ropers, Hans-Hilger, Frans P. M. Cremers

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Towards comprehensive identification and functional characterization of deep-intronic ABCA4 variants in 1000 Stargardt disease cases von Khan, M, Cornelis, S, Valero, MD, Khan, MI, Stohr, H, Grassmann, F, Steehouwer, M, Hoischen, A, Ayuso, C, Ramesar, R, Meunier, IA, Defoort, S, Weber, BHF, Dhaenens, CM, Cremers, FP

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OR11-002 - Mutations in MVK cause non-syndromic RP von Siemiatkowska, AM, Stoffels, M, Neveling, K, Simon, A, van Hagen, PM, den Hollander, AI, Cremers, FP, van den Born, LI, Collin, RW

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Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1 von Arno, G, Hull, S, Carss, K, Dev-Borman, A, Chakarova, C, Bujakowska, K, van den Born, I, Robson, AG, Holder, GE, Michaelides, M, Cremers, FP, Pierce, E, Raymond, FL, Moore, AT, Webster, AR

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Combined remote mineralogical and elemental identification from rovers: Field and laboratory tests using reflectance and laser-induced breakdown spectroscopy von Wiens, Roger C., Arvidson, Raymond E., Cremers, David A., Ferris, Monty J., Blacic, James D., Seelos IV, Frank P., Deal, Kim S.

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