Correction of the Splicing Defect Caused by a Recurrent Variant in ABCA4 (c.769-784C>T) That Underlies Stargardt Disease

Stargardt disease is an inherited retinal disease caused by biallelic mutations in the ABCA4 gene, many of which affect ABCA4 splicing. In this study, nine antisense oligonucleotides (AONs) were designed to correct pseudoexon (PE) inclusion caused by a recurrent deep-intronic variant in ABCA4 (c.769...

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Detalles Bibliográficos
Autores principales: Tomkiewicz, Tomasz Z., Nieuwenhuis, Sara E., Cremers, Frans P. M., Garanto, Alejandro, Collin, Rob W. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777113/
https://www.ncbi.nlm.nih.gov/pubmed/36552712
http://dx.doi.org/10.3390/cells11243947

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9777113/
https://www.ncbi.nlm.nih.gov/pubmed/36552712
http://dx.doi.org/10.3390/cells11243947

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