Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation.

Metab Brain Dis · 2020 · PMC7584531 · PMID 32740724

Europe PMC DOI

hedged sentence

0.0570

closest p · 1.1× alpha

0.0570

boldest claim

The sentences

borderline significantp = 0.057so close (0.05 < p ≤ 0.1)

Only a borderline significant difference was noted for haplogroup K and its marginally higher than expected prevalence in LHON patients compared to controls (11% vs 0%, p = 0.057).

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