Publikationen von Bax, Nathalie M.

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. und 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), S. 1751-1760. Volltext nicht vorhanden.

Lambertus, Stanley , Lindner, Moritz , Bax, Nathalie M., Mauschitz, Matthias M., Nadal, Jennifer, Schmid, Matthias , Schmitz-Valckenberg, Steffen, den Hollander, Anneke I., Weber, Bernhard H. F. , Holz, Frank G., van der Wilt, Gert Jan, Fleckenstein, Monika und Hoyng, Carel B. (2016) Progression of Late-Onset Stargardt Disease. Investigative Opthalmology & Visual Science 57 (13), S. 5186.