Genetic variation in DLG5 is associated with inflammatory bowel disease-Reference-Cited by-同舟云学术

Genetic variation in DLG5 is associated with inflammatory bowel disease

Published:2004-04-11 Issue:5 Volume:36 Page:476-480
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Stoll Monika,Corneliussen Brit,Costello Christine M,Waetzig Georg H,Mellgard Bjorn,Koch W Andreas,Rosenstiel Philip,Albrecht Mario,Croucher Peter J P,Seegert Dirk,Nikolaus Susanna,Hampe Jochen,Lengauer Thomas,Pierrou Stefan,Foelsch Ulrich R,Mathew Christopher G,Lagerstrom-Fermer Maria,Schreiber Stefan

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1345.pdf

Reference17 articles.

1. Hugot, J.P. et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411, 599– 603 (2001).

2. Ogura, Y. et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411, 603– 606 (2001).

3. Hampe, J. et al. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 357, 1925– 1928 (2001).

4. Bonen, D.K. & Cho, J.H. The genetics of inflammatory bowel disease. Gastroenterology 124, 521– 536 (2003).

5. Hampe, J. et al. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. Am. J. Hum. Genet. 64, 808– 816 (1999).

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