Genotyping Microarray for CSNB-Associated Genes
Investigative Ophthalmology & Visual Science2009Vol. 50(12), pp. 5919–5919
Citations Over TimeTop 11% of 2009 papers
Christina Zeitz, Stephan Labs, Birgit Lorenz, U. Förster, Janne Üksti, Hester Y. Kroes, Elfride De Baere, Bart P. Leroy, Frans P.M. Cremers, Mariana Wittmer, Maria M. van Genderen, José‐Alain Sahel, Isabelle Audo, Charlotte M. Poloschek, Saddek Mohand‐Saïd, Johannes Fleischhauer, Ulrike Hüffmeier, Veselina Moskova‐Doumanova, Alex V. Levin, Christian P. Hamel, Dorothee Leifert, Francis L. Munier, Daniel F. Schorderet, Eberhart Zrenner, Christoph Friedburg, Bernd Wissinger, Susanne Kohl, Wolfgang Berger
Abstract
This relatively inexpensive first-pass genetic testing device for patients with a diagnosis of CSNB will improve molecular diagnostics and genetic counseling of patients and their families and gives the opportunity to analyze whether, for example, more progressive disorders such as cone or cone-rod dystrophies underlie the same gene defects.
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