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Gene therapy rescues cone function in congenital achromatopsia
The successful restoration of visual function with recombinant adeno-associated virus (rAAV)-mediated gene replacement therapy in animals and humans with an inherited disease of the retinal pigment epithelium has ushered in a new era of retinal therapeutics. For many retinal disorders, however, targ...
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| Hauptverfasser: | , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2010
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2883338/ https://ncbi.nlm.nih.gov/pubmed/20378608 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq136 |
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