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Superior human hepatocyte transduction with Adeno-associated Virus Vector Serotype 7
Although therapeutic outcomes have been achieved in hemophilia patients after delivery of clotting factor genes to the liver using adeno-associated virus (AAV) vectors, it is well known that the pre-clinical results generated from hemophilia animal models have not been directly predictive of success...
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| Vydáno v: | Gene Ther |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6923567/ https://ncbi.nlm.nih.gov/pubmed/31570819 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41434-019-0104-5 |
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