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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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Detalhes bibliográficos
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 em: Landes Bioscience 2010
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Acesso em linha: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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