SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis. (Q47923406)

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scientific article published on 12 March 2009
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SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis.
scientific article published on 12 March 2009

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    SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosis (English)

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