Barely Significant
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A novel SERPINA1 mutation causing serum alpha(1)-antitrypsin deficiency.

PLoS One · 2012 · PMC3520848 · PMID 23251618

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highly significantno p-value reported
Although the structural consequences of the T379Δ mutation are not immediately obvious, it is highly significant that the mutation introduces an entirely new, extended C-terminal sequence into α 1 AT.

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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.