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Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2(Dy-w) mice, a model for congenital muscular dystrophy type 1A
MDC1A, the second most prevalent form of congenital muscular dystrophy, results from laminin-α2 chain deficiency. This disease is characterized by extensive muscle wasting that results in extremely weak skeletal muscles. A large percentage of children with MDC1A are faced with respiratory as well as...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3098729/ https://ncbi.nlm.nih.gov/pubmed/21441569 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr126 |
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