Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

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Human Molecular Genetics, Vol. 18, Iss. 9, 2009-05 ,pp. : 1633-1641

Oxford University Press

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Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3

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Human Molecular Genetics, Vol. 8, Iss. 3, 1999-03 ,pp. : 471-479

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Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na v 1.6)

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Human Molecular Genetics, Vol. 11, Iss. 22, 2002-10 ,pp. : 2765-2775

Oxford University Press

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Severe Myoclonic Epilepsy in Infancy – Adult Phenotype with Bradykinesia, Hypomimia, and Perseverative Behavior: Report of Five Cases

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Molecular Syndromology, Vol. 1, Iss. 5, 2011-03 ,pp. : 231-238

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Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2

By Kearney Jennifer A.   Yang Yan   Beyer Barbara   Bergren Sarah K.   Claes Lieve   DeJonghe Peter   Frankel Wayne N.  

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