A study in three European IBD cohorts confirms that the ATG16L1 c.898A > G (p.Thr300Ala) variant is a susceptibility factor for Crohn's disease

Journal of Crohn's and Colitis

Volumn 1, Issue 2, 2007, Pages 70-76

  Büning, Carsten ^a   Durmus, Tahir ^a   Molnar, Tamas ^c   de Jong, Dirk J ^d   Drenth, Joost P H ^d   Fiedler, Thomas ^a   Gentz, Enno ^a   Todorov, Theodor ^a   Haas, Verena ^a   Buhner, Sabine ^e   Sturm, Andreas ^a   Baumgart, Daniel C ^a   Nagy, Ferenc ^c   Lonovics, Janos ^c   Landt, Olfert ^f   Kage, Andreas ^a   Büning, Herbert ^g   Nickel, Renate ^a   Büttner, Janine ^a   Lochs, Herbert ^a   Schmidt, Hartmut H J ^b   Witt, Heiko ^a   more..

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^c UNIVERSITY OF SZEGED   (Hungary)

^d RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^e TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^f TIB MOLBIOL   (Germany)

^g FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

ATG16L1; CARD15; Crohn's disease; Inflammatory bowel disease; Ulcerative colitis

Indexed keywords

ADULT; ARTICLE; CLINICAL ASSESSMENT; CLINICAL EXAMINATION; COHORT ANALYSIS; CONTROLLED STUDY; CROHN DISEASE; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; ENTERITIS; ETHNIC DIFFERENCE; FEMALE; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; GERMANY; HUMAN; HUNGARY; MAJOR CLINICAL STUDY; MALE; NETHERLANDS; OUTCOMES RESEARCH; PHENOTYPE; POPULATION RESEARCH; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; ULCERATIVE COLITIS;

EID: 37249054533     PISSN: 18739946     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.crohns.2007.08.001     Document Type: Article

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