1[1]Wang Q,Curran ME,Splawski I,et al.Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.Nat Genet,1996,12:17
2[2]Wang HS,Pan Z,Shi W,et al.KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.Science,1998,282:1890
3[3]Schroeder BC,Kubisch C,Stein V,et al.Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.Nature,1998,396:687
4[4]Biervert C,Schroeder BC,Kubisch C,et al.A potassium channel mutation in neonatal human epilepsy.Science,1998,279:403
5[5]Charlier C,Singh NA,Ryan SG,et al.A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.Nat Genet,1998,18:53
6[6]Singh NA,Charlier C,Stauffer D,et al.A novel potassium channel gene,KCNQ2,is mutated in an inherited epilepsy of newborns.Nat Gent,1998,18:25
7[7]Eunson LH,Rea R,Zuberi SM,et al.Clinical,genetic,and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.Ann Neurol,2000,48:647
8[8]Burgess DL,Kohrman DC,Galt J,et al.Mutation of a new sodium channel gene,Scn8a,in the mouse mutant motor endplate disease'.Nat Genet,1995,10:461
9[9]Kohrman DC,Smith MR,Goldin AL,et al.A missense mutation in the sodium channel Scn8a is responsible for the cerebellar ataxia in the mouse mutant jolting.J Neurosci,1996,16:5993
10[10]Scheffer IE,Berkovic SF.Generalized epilepsy with febrile seizures plus-a genetic disorder with heterogeneous clinical phenotypes.Brain,1997,120:479