A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A (Q58417059)

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scientific article published on 01 September 2006
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A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
scientific article published on 01 September 2006

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    A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A (English)

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