Wordt geladen...
Pharmacologic Management of Duchenne Muscular Dystrophy: Target Identification and Preclinical Trials
Duchenne muscular dystrophy (DMD) is an X-linked human disorder in which absence of the protein dystrophin causes degeneration of skeletal and cardiac muscle. For the sake of treatment development, over and above definitive genetic and cell-based therapies, there is considerable interest in drugs th...
Bewaard in:
| Hoofdauteurs: | , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2014
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4158345/ https://ncbi.nlm.nih.gov/pubmed/24936034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ilar/ilu011 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|