Prevalence of mutations in inherited retinal diseases: A comparison between the United States and India.

Mol Genet Genomic Med · 2020 · PMC7005662 · PMID 31816670

Europe PMC DOI

hedged sentence

0.0600

closest p · 1.2× alpha

0.0600

boldest claim

The sentences

approaches statistical significancep = .06so close (0.05 < p ≤ 0.1)

Although the numbers are small, the difference in definitive diagnosis is statistically different from the Indian cohort ( p = .01) and the difference in definitive and indeterminate diagnosis approaches statistical significance ( p = .06) supporting a lower diagnostic rate in underrepresented ethnicities (Carss et al., 2017 ).

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