Condition: Generalized Epilepsy and Paroxysmal Dyskinesia
rs137853333
in
KCNMA1
gene and
Generalized Epilepsy and Paroxysmal Dyskinesia
PMID 26195193
2015 De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.
PMID 15937479
2005 Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.