Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.

PLoS One · 2012 · PMC3391281 · PMID 22792389

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highly significantno p-value reported

Also, rs7978987 in STX2 had a highly significant P value of 3.82×10 −11 in this meta-analysis.

also in 132,142 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.