A missense variant in SLC39A8 is associated with severe idiopathic scoliosis.

Nat Commun · 2018 · PMC6177404 · PMID 30301978

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highly significantno p-value reported

Discussion We identified a highly significant association between a coding variant in the manganese transporter SLC39A8 and risk of adolescent idiopathic scoliosis.

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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.