A Novel Screening Approach for Familial Hypercholesterolemia: A Genetic Study on Patients Detected Using Preexisting Centralized Analytics.

J Clin Med · 2025 · PMC12027611 · PMID 40283609

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did not reach statistical significanceno p-value reported

In our cohort, null allele variants tended to exhibit higher total and LDL-C levels than defective variants, although this difference did not reach statistical significance probably due to the limited sample size.

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