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Laminin Alters Fyn Regulatory Mechanisms and Promotes Oligodendrocyte Development
Mutations in LAMA2, the gene for the extracellular matrix protein laminin-α2, cause a severe muscular dystrophy termed congenital muscular dystrophy type-1A (MDC1A). MDC1A patients have accompanying CNS neural dysplasias and white matter abnormalities for which the underlying mechanisms remain unkno...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Society for Neuroscience
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2789400/ https://ncbi.nlm.nih.gov/pubmed/19776266 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0888-09.2009 |
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