Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy. (Q50892535)

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scientific article published on 20 July 2012
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Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.
scientific article published on 20 July 2012

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    Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy (English)

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