The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy.

Nat Commun · 2019 · PMC6531493 · PMID 31118417

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highly significantno p-value reported

Bonferroni’s highly significant difference (HSD) post hoc analysis was used for multiple pairwise comparison.

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