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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Detalles Bibliográficos
Autores principales: Boyer, Justin G, Murray, Lyndsay M, Scott, Kyle, De Repentigny, Yves, Renaud, Jean-Marc, Kothary, Rashmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852932/
https://www.ncbi.nlm.nih.gov/pubmed/24119341
http://dx.doi.org/10.1186/2044-5040-3-24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852932/
https://www.ncbi.nlm.nih.gov/pubmed/24119341
http://dx.doi.org/10.1186/2044-5040-3-24

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