Identification of genetic susceptibility loci for intestinal Behçet's disease.

Sci Rep · 2017 · PMC5206652 · PMID 28045058

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failed to reach significanceno p-value reported

Haplotype analysis suggested phospholipase C beta 1 ( PLCB1 ), transforming growth factor, beta receptor 3 ( TGFBR3 ), DDB1 and CUL4 associated factor 12 ( DCAF12 ), and schwannomin interacting protein 1 ( SCHIP1 ) as potential causal variants of intestinal BD, although they failed to reach significance in the Bonferroni test in a replication study ( Supplementary information 4 ).

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