Show 250 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="Pott, Jan-Willem R" or (type any "bookEditor issueEditor" and editor="Pott, Jan-Willem R") Add to list Journal Article A1 open access Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, Esmee H Runhart, Miriam Bauwens (UGent) , Nathalie M Bax, L Ingeborgh van den Born, Muhammad Imran Khan, Stéphanie S Cornelis, Joke BGM Verheij, et al. (2019) GENETICS IN MEDICINE. 21(8). p.1751-1760 Add to list Journal Article A1 open access Clinical characterization of 66 patients with congenital retinal disease due to the deep-intronic c.2991+1655A>G mutation in CEP290 Dyon Valkenburg, Caroline Van Cauwenbergh (UGent) , Birgit Lorenz, Mies M van Genderen, Mette Bertelsen, Jan-Willem R Pott, Frauke Coppieters (UGent) , Julie De Zaeytijd (UGent) , Alberta AHJ Thiadens, Caroline CW Klaver, et al. (2018) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 59(11). p.4384-4391 Add to list Journal Article A1 Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy Alberta AHJ Thiadens, T My Lan Phan, Renate C Zekveld-Vroon, Bart Leroy (UGent) , L Ingeborgh van den Born, Crel B Hoyng, Caroline CW Klaver, Susanne Roosing, Jan-Willem R Pott, Mary J van Schooneveld, et al. (2012) OPHTHALMOLOGY. 119(4). p.819-826