Barely Significant
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Clinical Phenotype and Inheritance in Patients With C9ORF72 Hexanucleotide Repeat Expansion: Results From a Large French Cohort.

Front Neurosci · 2020 · PMC7199526 · PMID 32410933

Europe PMCDOI
2
hedged sentences
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp < 0.0001actually significant
65.7 years, which was highly significant ( p < 0.0001).

also in 132,142 other papers

somewhat significantno p-value reported
The cohort represents the recruitment of an ALS center, and it is possible that another source of recruitment, such as an FTD expert center for example, could have a somewhat significant clinical spectrum to describe.

also in 217 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.