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...

Descripción completa

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

Ejemplares similares

Ejemplares similares