Oxidative stress, a new hallmark in the pathophysiology of Lafora progressive myoclonus epilepsy.


Lafora disease (LD; OMIM 254780, ORPHA501) is a devastating neurodegenerative disorder characterized by the presence of glycogen-like intracellular inclusions called Lafora bodies and caused, in most cases, by mutations in either the EPM2A or the EPM2B gene, encoding respectively laforin, a phosphatase with dual specificity that is involved in the… (More)
DOI: 10.1016/j.freeradbiomed.2015.01.034


Figures and Tables

Sorry, we couldn't extract any figures or tables for this paper.

Blog articles referencing this paper