Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
BACKGROUND: A German genome-wide nonsynonymous single nucleotide polymorphism (nsSNP) association study identified ATG16L1 as a Crohn's disease (CD) susceptibility gene. The association appeared to be confined to the nsSNP rs2,241,880 and was confirmed in 2 German independent case-control coll...
Main Authors: | Cummings, JR, Cooney, R, Pathan, S, Anderson, C, Barrett, J, Beckly, J, Geremia, A, Hancock, L, Guo, C, Ahmad, T, Cardon, L, Jewell, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2007
|
Similar Items
-
The genetics of NOD-like receptors in Crohn's disease.
by: Cummings, JR, et al.
Published: (2010) -
Association between genetic variants in myosin IXB and Crohn's disease.
by: Cooney, R, et al.
Published: (2009) -
Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
by: Cummings, JR, et al.
Published: (2007) -
Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease.
by: Beckly, J, et al.
Published: (2008) -
Confirmation of the novel association at the BTNL2 locus with ulcerative colitis.
by: Pathan, S, et al.
Published: (2009)