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Characterization of brain dystrophins absence and impact in dystrophin-deficient Dmd(mdx) rat model
Duchenne Muscular Dystrophy (DMD) is a severe muscle-wasting disease caused by mutations in the DMD gene encoding dystrophin, expressed mainly in muscles but also in other tissues like retina and brain. Non-progressing cognitive dysfunction occurs in 20 to 50% of DMD patients. Furthermore, loss of e...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7065776/ https://ncbi.nlm.nih.gov/pubmed/32160266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0230083 |
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