Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.

PLoS One · 2012 · PMC3340342 · PMID 22558438

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showed a trendno p-value reported

Genetic analysis of the codon 129 methionine/valine (M/V) polymorphism in all patients with sporadic CJD (sCJD) showed a trend for under-representation of VV cases (7.0%), compared with sCJD cohorts in other Western countries, whereas the MV genotype was relatively over-represented (22,4%).

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