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Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora Disease
Lafora disease (LD), the most devastating adolescence-onset epilepsy, is caused by mutations in the EPM2A or EPM2B genes, which encode the proteins laforin and malin, respectively. Loss of function of one of these proteins, which are involved in the regulation of glycogen synthesis, induces the accu...
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| Publicado no: | Glia |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6240358/ https://ncbi.nlm.nih.gov/pubmed/30152044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/glia.23463 |
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