Barely Significant
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Genetic variability of <i>FOXP2</i> and its targets <i>CNTNAP2</i> and <i>PRNP</i> in frontotemporal dementia: A pilot study in a southern Italian population.

Heliyon · 2024 · PMC11140708 · PMID 38828303

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nominally significantno p-value reported
Finally, we performed a conditional logistic regression analysis for testing if the effects of the two nominally significant SNPs (rs17213159 and rs1023073) showed independent effects.

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