Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

Nature Genetics

Volumn 29, Issue 2, 2001, Pages 223-228

  Rioux, John D ^a   Daly, Mark J ^a   Silverberg, Mark S ^b   Lindblad, Kerstin ^a   Steinhart, Hillary ^b   Cohen, Zane ^b   Delmonte, Terrye ^a   Kocher, Kerry ^a   Miller, Katie ^a   Guschwan, Sheila ^a   Kulbokas, Edward J ^a   O'Leary, Sinead ^a   Winchester, Ellen ^a   Dewar, Ken ^a   Green, Todd ^a   Stone, Valerie ^a   Chow, Christine ^a   Cohen, Albert ^c   Langelier, Diane ^d   Lapointe, Gilles ^e   Gaudet, Daniel ^e   Faith, Janet ^c   Branco, Nancy ^c   Bull, Shelley B ^b   Mcleod, Robin S ^b   Griffiths, Anne M ^b   Bitton, Alain ^c   Greenberg, Gordon R ^b   Lander, Eric S ^a,f   Siminovitch, Katherine A ^b   Hudson, Thomas J ^a,c   more..

^a WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^b MOUNT SINAI HOSPITAL   (Canada)

^c MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^d CENTRE HOSPITALIER UNIVERSITAIRE DE SHERBROOKE   (Canada)

^e Department of Pediatrics and Clinical Research Unit   (Canada)

^f MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE;

ARTICLE; CHROMOSOME 5Q; CROHN DISEASE; GENE CLUSTER; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENE MAPPING; GENE STRUCTURE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; CROHN DISEASE; CYTOKINES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; MULTIGENE FAMILY; POLYMORPHISM, SINGLE NUCLEOTIDE; VARIATION (GENETICS);

EID: 0034785352     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1001-223     Document Type: Article

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