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CRISPR applications for Duchenne muscular dystrophy: From animal models to potential therapies
CRISPR gene‐editing technology creates precise and permanent modifications to DNA. It has significantly advanced our ability to generate animal disease models for use in biomedical research and also has potential to revolutionize the treatment of genetic disorders. Duchenne muscular dystrophy (DMD)...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley & Sons, Inc.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078488/ https://www.ncbi.nlm.nih.gov/pubmed/35909075 http://dx.doi.org/10.1002/wsbm.1580 |