Proteomic assessment of a cell model of spinal muscular atrophy

BACKGROUND: Deletion or mutation(s) of the survival motor neuron 1 (SMN1) gene causes spinal muscular atrophy (SMA), a neuromuscular disease characterized by spinal motor neuron death and muscle paralysis. Complete loss of the SMN protein is embryonically lethal, yet reduced levels of this protein r...

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Detalles Bibliográficos
Autores principales: Wu, Chia-Yen, Whye, Dosh, Glazewski, Lisa, Choe, Leila, Kerr, Douglas, Lee, Kelvin H, Mason, Robert W, Wang, Wenlan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063191/
https://www.ncbi.nlm.nih.gov/pubmed/21385431
http://dx.doi.org/10.1186/1471-2202-12-25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3063191/
https://www.ncbi.nlm.nih.gov/pubmed/21385431
http://dx.doi.org/10.1186/1471-2202-12-25

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