Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Cell |
|---|---|
| Prif Awduron: | , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2020
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| Pynciau: | |
| Mynediad Ar-lein: | 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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