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CRISPR-Cas9 for in vivo Gene Therapy: Promise and Hurdles
Owing to its easy-to-use and multiplexing nature, the genome editing tool CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats (CRISPR) associated nuclease 9) is revolutionizing many areas of medical research and one of the most amazing areas is its gene therapy potentials. Previou...
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| Publicado no: | Mol Ther Nucleic Acids |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5023403/ https://ncbi.nlm.nih.gov/pubmed/28131272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mtna.2016.58 |
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