DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
LinksClose Window
References
Sangermano R, Garanto A, Khan M. et al.
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.
Genet Med 2019;
DOI: 10.1038/s41436-018-0414-9.
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.