Condition: Epilepsy, Nocturnal Frontal Lobe, Type 1
rs121909580
in
CHRNA4
gene and
Epilepsy, Nocturnal Frontal Lobe, Type 1
PMID 7550350
1995 A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
PMID 14623738
2003 A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.
PMID 10563623
1999 A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy.