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Publication
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Journal Contribution - Journal Article
Journal: GENETICS IN MEDICINE
ISSN: 1530-0366
Issue: 8
Volume: 21
Pages: 1751 - 1760
Publication year:2019
BOF-keylabel:yes
IOF-keylabel:yes
BOF-publication weight:6
CSS-citation score:4
Authors:International
Authors from:Higher Education
Accessibility:Open