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Loss of GABAergic cortical neurons underlies the neuropathology of Lafora disease
BACKGROUND: Lafora disease is an autosomal recessive form of progressive myoclonic epilepsy caused by defects in the EPM2A and EPM2B genes. Primary symptoms of the pathology include seizures, ataxia, myoclonus, and progressive development of severe dementia. Lafora disease can be caused by defects i...
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Formato: | Artigo |
Idioma: | Inglês |
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BioMed Central
2014
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Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3917365/ https://ncbi.nlm.nih.gov/pubmed/24472629 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-6606-7-7 |
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