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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Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions

By Meisler Miriam H.   Plummer Nicholas W.   Burgess Daniel L.   Buchner David A.   Sprunger Leslie K.  

Genetica, Vol. 122, Iss. 1, 2004-09 ,pp. : 37-45

Springer Publishing Company

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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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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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Novel ENU-induced eye mutations in the mouse: models for human eye disease

By Brown S.D.M.  

Human Molecular Genetics, Vol. 11, Iss. 7, 2002-04 ,pp. : 755-767

Oxford University Press

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