Familial cortical myoclonus with a mutation in NOL3
Annals of Neurology , 06/15/2012
Russell JF et al. – The authors propose that Familial Cortical Myoclonus (FCM) is a novel movement disorder that may be caused by mutation in NOL3. Further investigation of the role of NOL3 in neuronal physiology may shed light on neuronal membrane hyperexcitability and pathophysiology of myoclonus and related disorders.