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Inflammation in Lafora Disease: evolution with disease progression in laforin and malin knock-out mouse models
Lafora progressive myoclonus epilepsy (Lafora disease, LD) is a fatal rare autosomal recessive neurodegenerative disorder characterized by the accumulation of insoluble ubiquitinated polyglucosan inclusions in the cytoplasm of neurons, which is most commonly associated with mutations in two genes: E...
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| Publicado no: | Mol Neurobiol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5472678/ https://ncbi.nlm.nih.gov/pubmed/27041370 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-016-9884-4 |
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