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Biomarkers in Duchenne Muscular Dystrophy: Current Status and Future Directions
Duchenne muscular dystrophy is a severe, X-linked disease characterized by decreased muscle mass and function in children. Genetic and biochemical research over the years has led to the characterization of the cause and the pathophysiology of the disease. Moreover, the elucidation of genetic mechan...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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IOS Press
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657716/ https://www.ncbi.nlm.nih.gov/pubmed/37545256 http://dx.doi.org/10.3233/JND-221666 |