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CRISPR/Cas9: a tool to eradicate HIV-1
The development of antiretroviral therapy (ART) has been effective in suppressing HIV replication. However, severe drug toxicities due to the therapy and its failure in targeting the integrated proviral genome have led to the introduction of a new paradigm of gene-based therapies. With its effective...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713993/ https://www.ncbi.nlm.nih.gov/pubmed/36457057 http://dx.doi.org/10.1186/s12981-022-00483-y |