Crohn’s disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene

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Aug 21, 2005 (publication date) through Sep 26, 2024

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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

Clinical Research

World J Gastroenterol. Aug 21, 2005; 11(31): 4833-4837
Published online Aug 21, 2005. doi: 10.3748/wjg.v11.i31.4833

Table 5 Distributions of three UGT1A7 haplotypes among study subjects

Haplotype	SNP	Number (%) of subjects with haplotype
		UC (allele = 190)	CD (allele = 120)	Control (allele = 400)
UGT1A71*	None	120 (63.2)	69 (57.5)	242 (60.5)
UGT1A72*	T387G, C391A, G392A	29 (15.3)	24 (20.0)	55 (13.8)
UGT1A73*	T387G, C391A, G392A,	41 (21.6)	27 (22.5)	103 (25.7)
	T622C
UGT1A74*	T622C	0 (0)	0 (0)	0 (0)

Citation: Machida H, Tsukamoto K, Wen CY, Shikuwa S, Isomoto H, Mizuta Y, Takeshima F, Murase K, Matsumoto N, Murata I, Kohno S, Wen CY. Crohn’s disease in Japanese is associated with a SNP-haplotype of N-acetyltransferase 2 gene. World J Gastroenterol 2005; 11(31): 4833-4837
URL: https://www.wjgnet.com/1007-9327/full/v11/i31/4833.htm
DOI: https://dx.doi.org/10.3748/wjg.v11.i31.4833