Huntington's disease: the case for genetic modifiers.

Genome Med · 2009 · PMC2768966 · PMID 19725930

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marginally significantno p-value reported

In others, a follow-up study has trended in the same direction or yielded marginally significant findings ( TCERG1 , GRIN2A ) [ 41 ].

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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.