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From diagnosis to therapy in Duchenne muscular dystrophy
Genetic approaches for the diagnosis and treatment of inherited muscle diseases have advanced rapidly in recent years. Many of the advances have occurred in the treatment of Duchenne muscular dystrophy (DMD), a muscle wasting disease where affected boys are typically wheelchair bound by age 12 years...
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| Gepubliceerd in: | Biochem Soc Trans |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Portland Press Ltd.
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7329342/ https://ncbi.nlm.nih.gov/pubmed/32597486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BST20190282 |
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