De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin (Q57905641)

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scientific article published on 08 July 2009
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De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
scientific article published on 08 July 2009

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    De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin (English)

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