Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy
The childhood neuromuscular disease spinal muscular atrophy (SMA) is caused by mutations or deletions of the survival motor neuron (SMN1) gene. Although SMA has traditionally been considered a motor neuron disease, the muscle-specific requirement for SMN has never been fully defined. Therefore, the...
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| Main Authors: | , , , , , |
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| 格式: | Artigo |
| 语言: | 英语 |
| 出版: |
2013
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| 在线阅读: | https://doi.org/10.1186/2044-5040-3-24 https://skeletalmusclejournal.biomedcentral.com/counter/pdf/10.1186/2044-5040-3-24 |
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