Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

Nat Commun · 2017 · PMC5379100 · PMID 28358029

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highly significantno p-value reported

From each region we chose two or more SNPs for replication: the most significant SNP plus one or more additional SNPs and, where available, highly significant exonic variants.

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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.