Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

PLoS One · 2018 · PMC5794141 · PMID 29389944

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failed to reach significanceno p-value reported

Similarly to these reports, the MAF of rs868875 was increased in the present study population (5.8%; P = 0.10) though the increase failed to reach significance.

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