Genetic variation in DLG5 is associated with inflammatory bowel disease

Nature Genetics

Volumn 36, Issue 5, 2004, Pages 476-480

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

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^b ASTRAZENECA R AND D   (Sweden)

^c Conaris Research Institute AG ^*  (Germany)

^d MAX PLANCK INSTITUTE FOR INFORMATICS   (Germany)

^e UNIVERSITY OF KIEL   (Germany)

^f KING'S COLLEGE LONDON   (United Kingdom)

^g Genetic Epidemiology of Vascular Disorders   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN DLG5; UNCLASSIFIED DRUG;

ALLELISM; AMINO ACID SUBSTITUTION; ARTICLE; CHROMOSOME 10Q; CONTROLLED STUDY; CROHN DISEASE; FEMALE; GENE INTERACTION; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC LINKAGE; GENETIC RISK; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; ULCERATIVE COLITIS;

ALLELES; AMINO ACID SUBSTITUTION; CARRIER PROTEINS; CASE-CONTROL STUDIES; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; CLONING, MOLECULAR; COHORT STUDIES; COLITIS, ULCERATIVE; CROHN DISEASE; EUROPE; FEMALE; GENOTYPE; HAPLOTYPES; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEMBRANE PROTEINS; NOD2 SIGNALING ADAPTOR PROTEIN; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; TUMOR SUPPRESSOR PROTEINS; VARIATION (GENETICS);

EID: 2442519456     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1345     Document Type: Article

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