Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.

Sci Rep · 2017 · PMC5473861 · PMID 28623311

Europe PMC DOI

hedged sentence

0.2100

closest p · 4.2× alpha

0.2100

boldest claim

The sentences

failed to reach statistical significanceP = 0.21not close (p > 0.1)

Although the frequency in the sporadic MS population was increased in comparison to the control population this difference failed to reach statistical significance (Chi-square test P = 0.21).

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