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Laforin-malin complex degrades polyglucosan bodies in concert with glycogen debranching enzyme and brain isoform glycogen phosphorylase
In Lafora disease (LD), deficiency of either EPM2A or NHLRC1, the genes encoding the phosphatase laforin and E3 ligase respectively, causes massive accumulation of less-branched glycogen inclusions, known as Lafora bodies, also called polyglucosan bodies (PBs), in several types of cells including ne...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3954894/ https://ncbi.nlm.nih.gov/pubmed/24068615 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-013-8546-z |
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