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Malin decreases glycogen accumulation by promoting the degradation of protein targeting to glycogen (PTG)
Lafora disease (LD) is an autosomal recessive neurodegenerative disease that results in progressive myoclonus epilepsy and death. LD is caused by mutations in either the E3 ubiquitin ligase malin or the dual-specificity phosphatase laforin. A hallmark of LD is the accumulation of insoluble glycogen...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2251628/ https://ncbi.nlm.nih.gov/pubmed/18070875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M708712200 |
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