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Detection of human survival motor neuron (SMN) protein in mice containing the SMN2 transgene: applicability to preclinical therapy development for spinal muscular atrophy

Spinal muscular atrophy (SMA), the leading genetic cause of infant death results from loss of spinal motor neurons causing atrophy of skeletal muscle. SMA is caused by loss of the Survival Motor Neuron 1 (SMN1) gene, however, an identically-coding gene called SMN2 is retained, but is alternatively s...

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Main Authors: Mattis, Virginia B., Butchbach, Matthew E. R., Lorson, Christian L.
Formato: Artigo
Idioma:Inglês
Publicado: 2008
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2613335/
https://ncbi.nlm.nih.gov/pubmed/18771690
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jneumeth.2008.07.024
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