NMDA receptor gene variations as modifiers in Huntington disease: a replication study.

PLoS Curr · 2011 · PMC3186947 · PMID 21989477

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hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

Yet, when subjects were stratified by AO subtypes, we found nominally significant evidence for an association of the GRIN2A rs1969060 variation and the GRIN2B rs1806201 variation.

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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.