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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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Dettagli Bibliografici
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Landes Bioscience 2010
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Accesso online: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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