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

By Papale Ligia A.   Beyer Barbara   Jones Julie M.   Sharkey Lisa M.   Tufik Sergio   Epstein Michael   Letts Verity A.   Meisler Miriam H.   Frankel Wayne N.   Escayg Andrew  

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

Oxford University Press

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Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Na v 1.6) and a genetically linkedretinal mutation, rd13

By Buchner David  

Mammalian Genome, Vol. 15, Iss. 5, 2004-05 ,pp. : 344-351

Springer Publishing Company

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The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy

By Martin Melinda S.   Tang Bin   Papale Ligia A.   Yu Frank H.   Catterall William A.   Escayg Andrew  

Human Molecular Genetics, Vol. 16, Iss. 23, 2007-12 ,pp. : 2892-2899

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

By Sprunger L.K.  

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

Oxford University Press

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

By Stevens M.J.  

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

Oxford University Press

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