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Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin gene leading to the absence of the corresponding RNA transcript and protein. Absence of dystrophin leads to disruption of the dystrophin-associated protein complex and substantial changes in skeletal muscle pathol...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2002
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC137534/ https://ncbi.nlm.nih.gov/pubmed/12415109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.192571199 |
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