Barely Significant
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Atypical Phenotype of Myotonic Dystrophy Type 1 with Variant Repeats at the Age of Diagnosis.

Biology (Basel) · 2026 · PMC13359955 · PMID 42450630

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nominally significantno p-value reported
Accordingly, nominally significant findings should be interpreted with caution and require confirmation in larger cohorts.

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