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Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
Spinal muscular atrophy (SMA) is a common pediatric neuromuscular disorder caused by insufficient levels of the survival of motor neuron (SMN) protein. Studies involving SMA patients and animal models expressing the human SMN2 gene have yielded relatively little information about the earliest cellul...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2722888/ https://ncbi.nlm.nih.gov/pubmed/18492800 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn156 |
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