Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

Lancet

Volumn 357, Issue 9272, 2001, Pages 1925-1928

  Hampe, Jochen ^a   Cuthbert, Andrew ^b   Croucher, Peter J P ^a   Mirza, Muddassar M ^b   Mascheretti, Silvia ^a   Fisher, Sheila ^b   Frenzel, Henning ^a   King, Kathy ^b   Hasselmeyer, Anja ^a   MacPherson, Andrew J S ^b   Bridger, Stephen ^b   Van Deventer, Sander ^c   Forbes, Alastair ^d   Nikolaus, Susanna ^a   Lennard Jones, John E ^d   Foelsch, Ulrich R ^a   Krawczak, Michael ^e   Lewis, Cathryn ^b   Schreiber, Stefan ^a   Mathew, Christopher G ^b  

^a UNIVERSITY OF KIEL   (Germany)

^b KING'S COLLEGE LONDON   (United Kingdom)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d ST MARK S HOSPITAL   (United Kingdom)

^e CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE;

ARTICLE; CONTROLLED STUDY; CROHN DISEASE; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; DNA POLYMORPHISM; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; ULCERATIVE COLITIS;

EID: 0035897904     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)05063-7     Document Type: Article

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