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Plasma lipidomic analysis shows a disease progression signature in mdx mice
Duchenne muscular dystrophy (DMD) is a rare genetic disorder affecting paediatric patients. The disease course is characterized by loss of muscle mass, which is rapidly substituted by fibrotic and adipose tissue. Clinical and preclinical models have clarified the processes leading to muscle damage a...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8217252/ https://ncbi.nlm.nih.gov/pubmed/34155298 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-92406-6 |
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