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Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy
The most common form of human congenital muscular dystrophy (CMD) is caused by mutations in the laminin-α2 gene. Loss of laminin-α2 function in this autosomal recessive type 1A form of CMD results in neuromuscular dysfunction and, often, early death. Laminin-α2–deficient skeletal muscles in both hum...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC529286/ https://ncbi.nlm.nih.gov/pubmed/15578095 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200422928 |
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