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Impaired autophagy in Lafora disease

Lafora disease (LD) is a progressive, lethal, autosomal recessive, neurodegenerative disorder that manifests with myoclonus epilepsy. LD is characterized by the presence of intracellular inclusion bodies called Lafora bodies (LB), in brain, spinal cord and other tissues. More than 50 percent of LD i...

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Main Authors: Knecht, Erwin, Aguado, Carmen, Sarkar, Sovan, Korolchuk, Viktor I, Criado-García, Olga, Vernia, Santiago, Boya, Patricia, Sanz, Pascual, Rodríguez de Córdoba, Santiago, Rubinsztein, David C
Formato: Artigo
Idioma:Inglês
Publicado: Landes Bioscience 2010
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3039746/
https://ncbi.nlm.nih.gov/pubmed/20818165
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/auto.6.7.13308
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