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Gene therapy for retinal disease

Gene therapy strategies for the treatment of inherited retinal diseases have made major advances in recent years. This review focuses on adeno-associated viral (AAV) vector approaches to treat retinal degeneration and thus prevent or delay the onset of blindness. Data from human clinical trials of g...

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Bibliografski detalji
Glavni autori: McClements, Michelle E, MacLaren, Robert E
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3831157/
https://ncbi.nlm.nih.gov/pubmed/23305707
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.trsl.2012.12.007
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