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Protein Degradation and Quality Control in Cells from Laforin and Malin Knockout Mice
Lafora disease is a progressive myoclonus epilepsy caused by mutations in the EPM2A or EPM2B genes that encode a glycogen phosphatase, laforin, and an E3 ubiquitin ligase, malin, respectively. Lafora disease is characterized by accumulation of insoluble, poorly branched, hyperphosphorylated glycogen...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4110273/ https://ncbi.nlm.nih.gov/pubmed/24914213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.580167 |
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