Genetics and pathogenesis of idiopathic scoliosis.

Scoliosis Spinal Disord · 2016 · PMC5125035 · PMID 27933320

Europe PMC DOI

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closest p

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boldest claim

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highly significantno p-value reported

Individual genotyping in 919 cases revealed a highly significant association with COL11A2 , which encodes a fibrillar collagen.

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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.