Association of DLG5 variants with gluten-sensitive enteropathy

Gut

Volumn 57, Issue 7, 2008, Pages 1027-1028

  Festen, E A ^a   Zhernakova, A ^b   Wijmenga, C ^a   Weersma, R K ^a  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CELIAC DISEASE; DLG5 GENE; ENTERITIS; GENE; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; INFLAMMATION; INTESTINE MUCOSA PERMEABILITY; LETTER; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ULCERATIVE COLITIS;

CASE-CONTROL STUDIES; CELIAC DISEASE; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MEMBRANE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; TUMOR SUPPRESSOR PROTEINS;

EID: 46349091751     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2007.144857     Document Type: Letter

References (4)

1. Van Bodegraven AA, Curley CR, Hunt K, et al. Genetic variation in myosin IXB is associated with ulcerative colitis. Gastroenterology 2006;131:1768-74.
2. Browning BL, Barclay ML, Bingham SA, et al. Gender-stratified analysis of DLG5 R30Q in 4707 Crohn's disease patients and 4973 controls from 12 Caucasian cohorts. J Med Genet 2008;45:36- 42.
3. Monsuur AJ, de Bakker PI, Alizadeh BZ, et al. Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect. Nat Genet 2005;37:1341-4.
4. Weersma RK, Stokkers PC, van Bodegraven AA, et al. A large, nationwide, case-control study for the association of DLG5, OCTN1/2 and CARD15 with inflammatory bowel diseases in the Netherlands [abstract]. Gastroenterology 2007;132:A445.