CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells

Mutations in the dystrophin gene cause Duchenne muscular dystrophy (DMD), which is characterized by lethal degeneration of cardiac and skeletal muscles. Mutations that delete exon 44 of the dystrophin gene represent one of the most common causes of DMD and can be corrected in ~12% of patients by edi...

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Detalles Bibliográficos
Autores principales: Min, Yi-Li, Li, Hui, Rodriguez-Caycedo, Cristina, Mireault, Alex A., Huang, Jian, Shelton, John M., McAnally, John R., Amoasii, Leonela, Mammen, Pradeep P. A., Bassel-Duby, Rhonda, Olson, Eric N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402849/
https://www.ncbi.nlm.nih.gov/pubmed/30854433
http://dx.doi.org/10.1126/sciadv.aav4324

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402849/
https://www.ncbi.nlm.nih.gov/pubmed/30854433
http://dx.doi.org/10.1126/sciadv.aav4324

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