Cargando...
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL ENDOGENOUS MURINE PARKIN MUTATION
Various mutations in the PARK2 gene which encodes the protein, parkin, are causal of a disease entity termed autosomal recessive juvenile parkinsonism. Parkin can function as an E3 ubiquitin protein ligase, mediating the ubiquitination of specific targeted proteins and resulting in proteasomal degra...
Guardado en:
| Autores principales: | , |
|---|---|
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2010
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2908247/ https://ncbi.nlm.nih.gov/pubmed/20089136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1471-4159.2010.06605.x |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|