Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.

Mol Genet Genomic Med · 2019 · PMC6625088 · PMID 31144463

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a nonsignificant trendno p-value reported

However, patients with a wildtype promoter‐haplotype on their unaffected SCN1A allele showed a nonsignificant trend for milder phenotypes.

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