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The Potential of CRISPR/Cas9 Gene Editing as a Treatment Strategy for Inherited Diseases
Clustered regularly interspaced short palindromic repeats (CRISPR) is a promising innovative technology for genomic editing that offers scientists the chance to edit DNA structures and change gene function. It has several possible uses consisting of editing inherited deficiencies, treating, and redu...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8715006/ https://www.ncbi.nlm.nih.gov/pubmed/34977000 http://dx.doi.org/10.3389/fcell.2021.699597 |