Condition: EPILEPSY, CHILDHOOD ABSENCE, 1


rs1057519201 in GABRB3 gene and EPILEPSY, CHILDHOOD ABSENCE, 1 PMID 28053010 2017 Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

PMID 28544625 2017 A mutation in GABRB3 associated with Dravet syndrome.