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Correction of muscular dystrophies by CRISPR gene editing
Muscular dystrophies are debilitating disorders that result in progressive weakness and degeneration of skeletal muscle. Although the genetic mutations and clinical abnormalities of a variety of neuromuscular diseases are well known, no curative therapies have been developed to date. The advent of g...
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| Publicat a: | J Clin Invest |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7259998/ https://ncbi.nlm.nih.gov/pubmed/32478678 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI136873 |
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