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

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)

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

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A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism

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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

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Springer Publishing Company

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