Genetics of prion diseases.

Curr Opin Genet Dev · 2013 · PMC3705206 · PMID 23518043

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

highly significantno p-value reported

Statistical analysis showed a modest association for Stmn2 but a highly significant association for the Rarb locus [ 31 •• ].

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