Condition: Epilepsy, Nocturnal Frontal Lobe, Type 4


rs1018084204 in CHRNA2 gene and Epilepsy, Nocturnal Frontal Lobe, Type 4 PMID 25847220 2015 Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy.

PMID 16826524 2006 Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear.

rs12721510 in CRH gene and Epilepsy, Nocturnal Frontal Lobe, Type 4 PMID 16222669 2005 Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene.