Precise genome editing with base editors
Single-nucleotide variants account for about half of known pathogenic genetic variants in human. Genome editing strategies by reversing pathogenic point mutations with minimum side effects have great therapeutic potential and are now being actively pursued. The emerge of precise and efficient genome...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
De Gruyter
2023-02-01
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| Series: | Medical Review |
| Assuntos: | |
| Acceso en liña: | https://doi.org/10.1515/mr-2022-0044 |
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