| 1 | GABRG2, GEFSP1, GEFSP2, SCB1A, SCN1B, SMEI2
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| Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
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| Scheffer IE, Zhang YH, Jansen FE, Dibbens L.
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| Brain Dev 31(5):394-400. Epub 2009 Feb 8. 2009
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| 2 | GEFSP1, SCN1B
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| Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations.
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| Scheffer IE, Harkin LA, Grinton BE, Dibbens LM, Turner SJ, Zielinski MA, Xu R, Jackson G, Adams J, Connellan M, Petrou S, Wellard RM, Briellmann RS, Wallace RH, Mulley JC, Berkovic SF.
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| Brain 130(Pt 1):100-9. Epub 2006 Oct 4.
2007
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| 3 | SCN1B, GEFSP1
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| Mutation in the Na+ channel subunit SCN1B produces paradoxical changes in peripheral nerve excitability.
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| Kiernan MC, Krishnan AV, Lin CS, Burke D, Berkovic SF.
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| Brain 128(Pt 8):1841-6. Epub 2005 Apr 27. 2005
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| 4 | SCN1B, GEFSP1
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| A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsy.
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| Audenaert D, Claes L, Ceulemans B, Lofgren A, Van Broeckhoven C, De Jonghe P.
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| Neurology 61(6):854-6. 2003
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| 5 | SCN1B, GEFSP1
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| Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1B.
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| Wallace RH, Scheffer IE, Parasivam G, Barnett S, Wallace GB, Sutherland GR, Berkovic SF, Mulley JC.
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| Neurology 58(9):1426-9. 2002
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| 6 | GEFSP1, SCN1B
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| Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
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| Wallace RH, et al.
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| Nat Genet 19 : 366-370. 1998
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| 7 | GEFSP1, SCN1B
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| Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.
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| Scheffer IE, Berkovic SF.
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| Brain 120 ( Pt 3):479-90. 1997
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