Barely Significant
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Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.

Brain · 2022 · PMC9014756 · PMID 35288744

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highly significantno p-value reported
Because the PRNP codon 129 MV genotype was a highly significant covariate, disease duration in each diagnostic group was also stratified depending on the genotype (the VV genotype was not considered due to the low number of cases).

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