1Chang BS, Lowenstein DH. Epilepsy. N Engl J Med, 2003,349:1257-1266.
2Mulley JC, Scheffer IE, Harkin LA, et al. Susceptibility genes for complex epilepsy. Hum Mol Genet, 2005,14:243-249.
3Fukuma G, Oguni H, Shirasaka Y, et al.Mutations of neuronal voltage-gated Na^+ channel α1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI(SMEB). Epilepsia ,2004,45 : 140-148.
4Castro PA, Cooper EC, Lowenstein DH, et al.Hippooampal heterotopia lack functional Kv4. 2 potassium channels in the methylazoxymethanol model of cortical malformations and epilepsy. J Neurosci ,2001,21:6626-6634.
5Pozo-Rosich P, Clover L, Saiz A, et al. Voltage-gated potassium channel antibodies in limbic encephalitis.Ann Neurol, 2003,54:530-533.
6Vincent A, Buckley C, Schott JM, et al.Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis.Brain ,2004,127:701-712.
7Lossin C, Wang DW, Rhodes TH, et al.Molecular basis of an inherited epilepsy. Neuron ,2002,34:877-884.
8Singh NA, Charlier C, Stauffer D, et aL A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.Nat Genet, 1998,18:25-29.
9Suzuki T, Delgado-Escueta AV, Aguan K, et al.Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet,2004,36:842-849.
10Wallace RH, Wang DW, Singh R, et al. Febrile seizures and generalized epilepsy associated with a mutation in the Na^+ -channel β1 subunit gene SCN1B. Nat Genet,1998,19:366-370.
