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A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori’s disease
Cori’s disease is a glycogen storage disorder characterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-α-glucanotransferase (AGL). Here, we demonstrate that the G1448R genetic variant of AGL is unable to bind to glycogen and displays decreased stability that is rescu...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2007
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1993871/ https://ncbi.nlm.nih.gov/pubmed/17908927 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.1553207 |
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