Barely Significant
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Clinical, electromyographic, and biophysical characterization of the rare Nav1.4 channel mutation <i>SCN4A</i> L1436P.

Front Physiol · 2025 · PMC12366458 · PMID 40843127

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indeterminate significanceno p-value reported
Case 9 was unique in presenting, in addition to the L1436P mutation, a c.5211dup (p.Tyr1738LeufsTer27) duplication of the SCN4A gene of indeterminate significance.

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