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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 en:Mol Neurobiol
Autores principales: López-González, Irene, Viana, Rosa, Sanz, Pascual, Ferrer, Isidre
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Acceso en línea: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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