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scn8a protein human
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Expanding the genotype-phenotype spectrum in SCN8A-related disorders.
Clinical features and genetic analysis of five children with epilepsies due to variants of SCN8A gen…
A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report.
The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Tre…
Clinical severity is correlated with age at seizure onset and biophysical properties of recurrent ga…
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