Effect of CYP2C19 polymorphisms on stiripentol administration in Japanese cases of Dravet syndrome

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A New Genetic Defect in Human CYP2C19: Mutation of the Initiation Codon Is Responsible for Poor Metabolism of S-Mephenytoin

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Mutations of Neuronal Voltage‐gated Na⁺ Channel α1 Subunit Gene <i>SCN1A</i> in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

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Joëlle Perez, Catherine Chiron, C. Musial et al. · Epilepsia · 1999 · 148 citations · Full text