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A Novel <i>SCN1A</i> Mutation: A Case Report.

J Pediatr Neurosci · 2020 · PMC7519752 · PMID 33042244

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may be significantno p-value reported
As new cases of this novel mutation are defined over time, the onset of afebrile seizures may be significant.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.