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CRISPR-Based Therapeutic Genome Editing: Strategies and In Vivo Delivery by AAV Vectors
The development of clustered regularly interspaced short-palindromic repeat (CRISPR)-based biotechnologies has revolutionized the life sciences and introduced new therapeutic modalities with the potential to treat a wide range of diseases. Here, we describe CRISPR-based strategies to improve human h...
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| Pubblicato in: | Cell |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7236621/ https://ncbi.nlm.nih.gov/pubmed/32243786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2020.03.023 |
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