Expanding the phenotypic spectrum of <i>TRAPPC11-</i>related muscular dystrophy: 25 Roma individuals carrying a founder variant.

J Med Genet · 2023 · PMC10579479 · PMID 37197784

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

highly significantno p-value reported

Progressive and highly significant microcephaly was almost universally found (21/23; 91%), being detected at birth in 38% of individuals and acquired during the first years of life in 52%.

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.