ONTOGENY OF LAFORA BODIES AND NEUROCYTOSKELETON CHANGES IN LAFORIN-DEFICIENT MICE

Lafora disease (LD) is an autosomal recessive, always fatal progressive myoclonus epilepsy with rapid cognitive and neurologic deterioration. One of the pathological hallmarks of LD is the presence of cytoplasmic PAS+ polyglucosan inclusions called Lafora bodies (LBs). Current clinical and neuropath...

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Bibliografiset tiedot
Päätekijät: Machado-Salas, Jesús, Avila-Costa, María Rosa, Guevara, Patricia, Guevara, Jorge, Durón, Reyna M., Bai, Dongsheng, Tanaka, Miyabi, Yamakawa, Kazuhiro, Delgado-Escueta, Antonio V.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3367664/
https://ncbi.nlm.nih.gov/pubmed/22542948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2012.04.008
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