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Use of imaging biomarkers to assess perfusion and glucose metabolism in the skeletal muscle of dystrophic mice
BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe neuromuscular disease that affects 1 in 3500 boys. The disease is characterized by progressive muscle degeneration that results from mutations in or loss of the cytoskeletal protein, dystrophin, from the glycoprotein membrane complex, thus in...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3141608/ https://ncbi.nlm.nih.gov/pubmed/21639930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2474-12-127 |
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