Gene: CHRNB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1141
Gene Symbol: CHRNB2
CHRNB2 		0.010 GeneticVariation disease BEFREE A case of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) coexisting with pervasive developmental disorder harboring SCN1A mutation in addition to CHRNB2 mutation. 23032131 2012