Condition: MYOCLONUS, FAMILIAL CORTICAL


rs397514600 in NOL3 gene and MYOCLONUS, FAMILIAL CORTICAL PMID 25138476 2014 Screening of mutations in NOL3 in a myoclonic syndromes series.

PMID 22926851 2012 Familial cortical myoclonus with a mutation in NOL3.