Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expression (Q36451955)

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Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expression
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    Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expression (English)
    Christopher H Thompson
    J Christopher Porter
    Kristopher M Kahlig
    Melissa A Daniels
    Alfred L George
    19 October 2012
    287
    42001-42008

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