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Adeno-associated virus vector as a platform for gene therapy delivery
Adeno-associated virus (AAV) vectors are the leading platform for gene delivery for the treatment of a variety of human diseases. Recent advances in developing clinically desirable AAV capsids, optimizing genome designs and harnessing revolutionary biotechnologies have contributed substantially to t...
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| Vydáno v: | Nat Rev Drug Discov |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6927556/ https://ncbi.nlm.nih.gov/pubmed/30710128 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41573-019-0012-9 |
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