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Emerging Issues in AAV-Mediated In Vivo Gene Therapy
In recent years, the number of clinical trials in which adeno-associated virus (AAV) vectors have been used for in vivo gene transfer has steadily increased. The excellent safety profile, together with the high efficiency of transduction of a broad range of target tissues, has established AAV vector...
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| Yayımlandı: | Mol Ther Methods Clin Dev |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society of Gene & Cell Therapy
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5758940/ https://ncbi.nlm.nih.gov/pubmed/29326962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.omtm.2017.11.007 |
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