Mitochondrial DNA sequence variation and neurodegeneration.

Hum Genomics · 2008 · PMC3525185 · PMID 19129091

Europe PMC DOI

hedged sentence

0.0100

closest p · 0.2× alpha

0.0100

boldest claim

The sentences

highly significantp < 0.01actually significant

In a comparison developed to investigate how haplogroup I differs from the other haplogroups tested, two nucleotides at positions 16391 and 10034 were identified; only the difference between 16391A and 10034C alleles was found to be highly significant ( p < 0.01) [ 48 ].

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