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Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA

Ocular gene therapy with recombinant adeno-associated virus (AAV) has shown vector-mediated gene augmentation to be safe and efficacious in the retina in one set of diseases (retinitis pigmentosa and Leber congenital amaurosis (LCA) caused by RPE65 deficiency), with excellent safety profiles to date...

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Autors principals: Scott J. Dooley, Devin S. McDougald, Krishna J. Fisher, Jeanette L. Bennicelli, Lloyd G. Mitchell, Jean Bennett
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2018-09-01
Col·lecció:Molecular Therapy: Nucleic Acids
Accés en línia:http://www.sciencedirect.com/science/article/pii/S2162253118301112
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