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Mutated SCN1A activates Panayiotopoulos syndrome 48. 1 / 1

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"43 Although the pathogenetic role of SCN1A mutations is increasingly recognised in familial hemiplegic migraine, 44,45 the hypothesis that SCN1A mutations might also underlie other epileptic condition[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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Mutated SCN1A activates Panayiotopoulos syndrome 48. 1 / 1

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