NOD2/CARD15 gene mutations in North Algerian patients with inflammatory bowel disease

doi:10.3748/wjg.v21.i25.7786

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Jul 7, 2015; 21(25): 7786-7794
Published online Jul 7, 2015. doi: 10.3748/wjg.v21.i25.7786

Table 4 Number of different genotypes observed in Crohn's disease/ulcerative colitis/healthy controls groups

Variant	p.Arg⁷⁰²Trp	p.Gly⁹⁰⁸Arg	p.Leu¹⁰⁰⁷fsinsC	WT
p.Arg⁷⁰²Trp	2/0/4	1/0/1	2/1/1	6/1/2
p.Gly⁹⁰⁸Arg		0/0/0	1/0/0	3/1/3
p.Leu¹⁰⁰⁷fsinsC			0/0/0	1/1/1
WT				70/42/102

In each cell of the table, the genotype is obtained by combining the two genetic variants indicated in the corresponding row and column. No patients homozygous for NOD2 gene p.Gly908Arg and p.Leu1007fsinsC mutations were found in this study. CD: Crohn's disease; UC: Ulcerative colitis; HC: Healthy controls; WT: Wild type.

Citation: Boukercha A, Mesbah-Amroun H, Bouzidi A, Saoula H, Nakkemouche M, Roy M, Hugot JP, Touil-Boukoffa C. NOD2/CARD15 gene mutations in North Algerian patients with inflammatory bowel disease. World J Gastroenterol 2015; 21(25): 7786-7794
URL: https://www.wjgnet.com/1007-9327/full/v21/i25/7786.htm
DOI: https://dx.doi.org/10.3748/wjg.v21.i25.7786