Condition: Benign Rolandic Epilepsy


rs118192212 in KCNQ2 gene and Benign Rolandic Epilepsy PMID 18640800 2009 A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.

PMID 22884718 2012 KCNQ2 abnormality in BECTS: benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2.

PMID 18625963 2008 KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.