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.