Condition: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3


rs121909672 in GABRG2 gene and GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 PMID 23708187 2013 Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

PMID 11326274 2001 First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.

PMID 16924025 2006 A novel GABRG2 mutation associated with febrile seizures.