Barely Significant
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Multifactorial etiology of progressive supranuclear palsy (PSP): the genetic component.

Acta Neuropathol · 2025 · PMC12137433 · PMID 40465013

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highly significantno p-value reported
Genetic association studies found highly significant association of polymorphic sequences in non-coding regions of MAPT with PSP, such as SNPs rs8070723 and rs242557 [ 43 , 81 ].

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