| 1 | BFNIS, SCN2A
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| SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.
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| Herlenius E, Heron SE, Grinton BE, Keay D, Scheffer IE, Mulley JC, Berkovic SF.
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| Epilepsia 48(6):1138-42. Epub 2007 Mar 26.
2007
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| 2 | ENFL1, CHRNA4, BRD2, ME2, LGI1, EPT, EFHC1, EJM1, BFNIS, SCN2A
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| Sacred disease secrets revealed: the genetics of human epilepsy.
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| Turnbull J, Lohi H, Kearney JA, Rouleau GA, Delgado-Escueta AV, Meisler MH, Cossette P, Minassian BA.
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| Hum Mol Genet 14(17):2491-500. Epub 2005 Jul 27. 2005
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| 3 | BFNIS,SCN2A
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| Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.
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| Bergren SK, Chen S, Galecki A, Kearney JA.
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| Mamm Genome 16(9):683-90. Epub 2005 Oct 19. 2005
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| 4 | BFNIS, SCN2A
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| Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.
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| Berkovic SF, Heron SE, Giordano L, Marini C, Guerrini R, Kaplan RE, Gambardella A, Steinlein OK, Grinton BE, Dean JT, Bordo L, Hodgson BL, Yamamoto T, Mulley JC, Zara F, Scheffer IE.
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| Ann Neurol 55(4):550-7. 2004
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