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Paper Details

Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.
Inflamm Bowel Dis
11
2016
CC 1, CC 2, Familial and Sporadic Inflammatory Bowel Disease, IBD, IBD-susceptibility gene, IL17REL, Il17REL Variants, UC, UC in, UC in CC 1, inflammatory bowel disease, patient, patients, rare variants, rs142430606, rs200958270, sporadic ulcerative colitis

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