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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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Detaylı Bibliyografya
Asıl Yazarlar: Worby, Carolyn A., Gentry, Matthew S., Dixon, Jack E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
Konular:
Online Erişim: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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