Human genetic variation and Parkinson's disease.

J Mov Disord · 2010 · PMC4027658 · PMID 24868370

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

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nominally significantno p-value reported

Importantly, the SNCA SNP rs2736990 is the same SNCA SNP that showed the second highest nominally significant association with PD susceptibility in the large-scale candidate association study of Chung et al.

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