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.