Barely Significant
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Multiple sclerosis and genetic polymorphisms in fibrinogen-mediated hemostatic pathways: a case-control study.

Neurol Sci · 2022 · PMC8918146 · PMID 34561786

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highly significantno p-value reported
Therefore, although the predictive values of the considered genetic variants are not backed by a highly significant statistic, our findings do not discount the involvement of these factors in MS pathogenesis and suggest evaluating these variants in a larger population-based cohort.

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