Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population.

Front Pediatr · 2018 · PMC6204400 · PMID 30406062

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

highly significantno p-value reported

We identified causative mutations in almost 40% of families with a family history of SRNS or CKD compared to only 6% of patients with SRNS and no family history, a difference that was highly significant and makes a positive family history of SRNS or CKD the single most important clinical predictor of mutation amongst patients with SRNS.

also in 132,142 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.