Lafora disease (LD) a fatal genetic type of myoclonic epilepsy is seen as a abnormally high degrees of cellular glycogen and its own accumulation seeing that Lafora bodies in MI 2 affected tissue. that mammalian focus on of rapamycin (mTOR) activates SGK1 kinase in laforin-deficient cells. The mTOR activation is apparently a glucose-dependent event and… Continue reading Lafora disease (LD) a fatal genetic type of myoclonic epilepsy is