Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy

BACKGROUND: 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. The...

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Bibliographische Detailangaben
Hauptverfasser: Boyer, Justin G, Murray, Lyndsay M, Scott, Kyle, De Repentigny, Yves, Renaud, Jean-Marc, Kothary, Rashmi
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2013
Schlagworte:
Research
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3852932/
https://ncbi.nlm.nih.gov/pubmed/24119341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2044-5040-3-24
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