Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis".

Ann Hum Genet · 2014 · PMC4240469 · PMID 24116917

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hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantP = 2.6 × 10 −7actually significant

The inheritance pattern shows a very highly significant deviation from the null hypothesis (χ 2 = 21.5; P = 2.6 × 10 −7 ) ( Table 1 ).

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