Condition: EPILEPSY, BENIGN NEONATAL, 2


rs118192213 in KCNQ2 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 17129708 2007 Benign familial neonatal convulsions: always benign?

PMID 12742592 2003 Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2.

rs118192192 in KCNQ2-AS1;KCNQ2 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 19464834 2009 Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.

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

rs118192248 in KCNQ3 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 20298421 2010 EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.

rs267607198 in LOC105372724;KCNQ2 gene and EPILEPSY, BENIGN NEONATAL, 2 PMID 15249611 2004 A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.