Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="ZEITZ, C" or (type any "bookEditor issueEditor" and editor="ZEITZ, C") Add to list Journal Article A1 open access A common NYX mutation in Flemish patients with X linked CSNB Bart Leroy (UGent) , BS Budde, M Wittmer, Elfride De Baere (UGent) , W Berger and C Zeitz (2009) BRITISH JOURNAL OF OPHTHALMOLOGY. 93(5). p.692-696 Add to list Journal Article A1 TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness I Audo, S Kohl, Bart Leroy (UGent) , FL Munier, X Guillonneau, S Mohand-Saïd, K Bujakowska, E Nandrot, B Lorenz, M Preising, et al. (2009) AMERICAN JOURNAL OF HUMAN GENETICS. 85(5). p.720-729 Add to list Journal Article A1 Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram C ZEITZ, M VAN GENDEREN, J NEIDHARDT, UFO LUHMANN, F HOEBEN, U FORSTER, K WYCISK, G MATYAS, CB HOYNG, F RIEMSLAG, et al. (2005) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 46(11). p.4328-4335