DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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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.
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