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)...

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Detalles Bibliográficos
Autores principales: Chey, Yu C. J., Arudkumar, Jayshen, Aartsma‐Rus, Annemieke, Adikusuma, Fatwa, Thomas, Paul Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Focus Article
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

Internet

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

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