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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Detaylı Bibliyografya
Asıl Yazarlar: Machado-Salas, Jesús, Avila-Costa, María Rosa, Guevara, Patricia, Guevara, Jorge, Durón, Reyna M., Bai, Dongsheng, Tanaka, Miyabi, Yamakawa, Kazuhiro, Delgado-Escueta, Antonio V.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2012
Konular:
Article
Online Erişim: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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