Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

113Citations
Citations of this article
31Readers
Mendeley users who have this article in their library.

Your institution provides access to this article.

Abstract

Crohn disease (CD) is an inflammatory bowel disease characterized by chronic transmural, segmental, and typically granulomatous inflammation of the gut. Recently, two novel candidate gene loci associated with CD, SLC22A4 and SLC22A5 on chromosome 5 known as IBD5 and DLG5 on chromosome 10, were identified through association analysis of Caucasian CD patients. We validated these candidate genes in Japanese patients with CD and found a weak but possible association with both SLC22A4 (P = 0.028) and DLG5 (P = 0.023). However, the reported genetic variants that were indicated to be causative in the Caucasian population were completely absent in or were not associated with Japanese CD patients. These findings imply significant differences in genetic background with CD susceptibility among different ethnic groups and further indicate some difficulty of population-based studies. © The Japan Society of Human Genetics and Springer-Verlag 2004.

Cite

CITATION STYLE

APA

Yamazaki, K., Takazoe, M., Tanaka, T., Ichimori, T., Saito, S., Iida, A., … Nakamura, Y. (2004). Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease. Journal of Human Genetics, 49(12), 664–668. https://doi.org/10.1007/s10038-004-0204-x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free