Localization of sequence variations in PGC-1α influence their modifying effect in Huntington disease.

Mol Neurodegener · 2011 · PMC3022537 · PMID 21211002

Europe PMC DOI

hedged sentence

0.0566

closest p · 1.1× alpha

0.0566

boldest claim

The sentences

marginally significantP = 0.0566so close (0.05 < p ≤ 0.1)

Apart from rs7665116 in the transcribed region of the PGC-1α gene, SNP rs2970870, located in the promoter region, showed a marginally significant effect on the HD AAO in the first analysis of covariance (P = 0.0566; Table 1 ).

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