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GENE AND CELL-MEDIATED THERAPIES FOR MUSCULAR DYSTROPHY
Duchenne muscular dystrophy (DMD) is a devastating muscle disorder that affects 1 in 3500 boys. Despite years of research and considerable progress in understanding the molecular mechanism of the disease and advancement of therapeutic approaches, there is no cure for DMD. The current treatment optio...
Bewaard in:
| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2013
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4077844/ https://ncbi.nlm.nih.gov/pubmed/23553671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mus.23738 |
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