1Turnbull J, Lohi H, Kearney JA, et al. Sacred Disease Secrets Revealed: The Genetics of Human Epilepsy. Hum Mol Genet, 2005, 14( 17): 2491-2500.
2Striano P, Bordo L, Lispi ML, et al. A novel SCN2A mutation in family with benign familial infantile seizures. Epilepsia,2006, 47(1) : 218-220.
3Audenaert D, Claes L, Claeys KG, et al. A novel susceptibility locus at 2p24 for generalized epilepsy with febrile seizures plus. J Med Genet, 2005, 42(12) : 947-952.
4Chen Y, Lu J, Pan H, et al. Association between genetic variation of CACNA 1 H and Childhood absence epilepsy. Ann Neurol, 2003, 54(2) : 239-243.
5Vitko I, Chen Y, Arias JM, et al. Functional characterization and neuronal modeling of the effects of childhood absence epilepsy variants of CACNA1 H, a T-type calcium channel. J Neurosci, 2005, 25(19): 4844-4855.
6Khosravani H, Alter C, Simms B, et al. Effects of Ca ( v ) 3.2 channel mutations linked to idiopathic generalized epilepsy.Ann Neurol, 2005, 57 (5) : 745-749.
7Suzuki T, Delgado-Escueta AV, Aguan K, et al. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet, 2004,36(8) : 842-849.
8Hua JY, Smear MC, Baier H, et al. Regulation of axon growth in vivo by activity-based competition. Nature, 2005,434(7036) : 1022-1026.
9Ottersen OP. Neurobiology: sculpted by competition. Nature,2005, 434(7036) : 969.
10Greenberg DA, Cayanis E, Strug L, et al. Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy. Am J Hum Genet, 2005, 76(1) : 139-146.