Axonal-SMN (a-SMN), a protein isoform of the survival motor neuron gene, is specifically involved in axonogenesis

Spinal muscular atrophy (SMA) is an autosomal recessive disease of childhood due to loss of the telomeric survival motor neuron gene, SMN1. The general functions of the main SMN1 protein product, full-length SMN (FL-SMN), do not explain the selective motoneuronal loss of SMA. We identified axonal-SM...

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Autors principals: Setola, Veronica, Terao, Mineko, Locatelli, Denise, Bassanini, Stefania, Garattini, Enrico, Battaglia, Giorgio
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2007
Matèries:
Biological Sciences
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1794299/
https://ncbi.nlm.nih.gov/pubmed/17261814
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0610660104
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