Browsing by Author "Sangermano, Riccardo"
Now showing 1 - 1 of 1
- Results Per Page
- Sort Options
Item Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides(2019-08) Sangermano, Riccardo; Garanto, Alejandro; Khan, Mubeen; Runhart, Esmee H.; Bauwens, Miriam; Bax, Nathalie M.; van den Born, L. Ingeborgh; Khan, Muhammad Imran; Cornelis, Stéphanie S.; Verheij, Joke B.G.M.; Pott, Jan Willem R.; Thiadens, Alberta A.H.J.; Klaver, Caroline C.W.; Puech, Bernard; Meunier, Isabelle; Naessens, Sarah; Arno, Gavin; Fakin, Ana; Carss, Keren J.; Raymond, F. Lucy; Webster, Andrew R.; Dhaenens, Claire Marie; Stöhr, Heidi; Grassmann, Felix; Weber, Bernhard H.F.; Hoyng, Carel B.; De Baere, Elfride; Albert, Silvia; Collin, Rob W.J.; Cremers, Frans P.M.; University of Aberdeen.Medical Sciences