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AAV Vectors for Efficient Gene Delivery to Rodent Hearts
Currently, gene therapy is one of the most promising fields in biomedicine, with great therapeutic potential for an array of inherited and acquired diseases. Adeno-associated viral (AAV) vectors have emerged as promising tools to deliver selectively a therapeutic payload to target organs, including...
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| Publicado no: | Methods Mol Biol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6586215/ https://ncbi.nlm.nih.gov/pubmed/30783983 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-9139-6_19 |
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