Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase von Kitiratschky, Veronique B.D, Behnen, Petra, Kellner, Ulrich, Heckenlively, John R, Zrenner, Eberhart, Jägle, Herbert, Kohl, Susanne, Wissinger, Bernd, Koch, Karl-Wilhelm

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Safety evaluation of “retina implant alpha IMS”—a prospective clinical trial von Kitiratschky, Veronique B. D., Stingl, Katarina, Wilhelm, Barbara, Peters, Tobias, Besch, Dorothea, Sachs, Helmut, Gekeler, Florian, Bartz-Schmidt, Karl Ulrich, Zrenner, Eberhart

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Mutation Analysis Identifies GUCY2D as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration von Kitiratschky, Veronique B. D, Wilke, Robert, Renner, Agnes B, Kellner, Ulrich, Vadala, Maria, Birch, David G, Wissinger, Bernd, Zrenner, Eberhart, Kohl, Susanne

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ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies von Kitiratschky, Veronique B D, Grau, Tanja, Bernd, Antje, Zrenner, Eberhart, Jägle, Herbert, Renner, Agnes B, Kellner, Ulrich, Rudolph, Günther, Jacobson, Samuel G, Cideciyan, Artur V, Schaich, Simone, Kohl, Susanne, Wissinger, Bernd

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