Barely Significant
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MYH7 Mutations in Restrictive Cardiomyopathy.

JACC Adv · 2025 · PMC12102527 · PMID 40286359

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a clear trendno p-value reported
13 The study cohort indicates a clear trend: individuals with pathogenic or likely pathogenic mutations have a greater prevalence of transplantation than those without such variants, emphasizing the genetic risk associated with transplantation.

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