The Phe932Ile mutation in KCNT1 channels associated with severe epilepsy, delayed myelination and leukoencephalopathy produces a loss-of-function channel phenotype
Keywords: ADNFLE; autosomal dominant nocturnal frontal lobe epilepsy; BSA; bovine serum albumin; EDTA; ethylenediaminetetraacetic acid; EGTA; ethylene glycol-bis(β-aminoethyl ether)-N,N,Nâ²,Nâ²-tetraacetic acid); EIMFS; epilepsy of infancy with migrating focal s