Items where Author is "Naessens, Sarah"

Article

Sangermano, Riccardo and Garanto, Alejandro and Khan, Mubeen and Runhart, Esmee H. and Bauwens, Miriam and Bax, Nathalie M. and van den Born, L. Ingeborgh and Khan, Muhammad Imran and Cornelis, Stephanie S. and Verheij, Joke B. G. M. and Pott, Jan-Willem R. and Thiadens, Alberta A. H. J. and Klaver, Caroline C. W. and Puech, Bernard and Meunier, Isabelle and Naessens, Sarah and Arno, Gavin and Fakin, Ana and Carss, Keren J. and Raymond, F. Lucy and Webster, Andrew R. and Dhaenens, Claire-Marie and Stoehr, Heidi and Grassmann, Felix and Weber, Bernhard H. F. and Hoyng, Carel B. and De Baere, Elfride and Albert, Silvia and Collin, Rob W. J. and Cremers, Frans P. M. (2019) Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides. GENETICS IN MEDICINE, 21 (8). pp. 1751-1760. ISSN 1098-3600, 1530-0366