Polymorphisms in the IBD5 locus are associated with crohn disease in pediatric ashkenazi jewish patients

Journal of Pediatric Gastroenterology and Nutrition

Volumn 48, Issue 5, 2009, Pages 531-537

  Tomer, Gitit ^a,b   Wetzler, Graciela ^b   Keddache, Mehdi ^c   Denson, Lee A ^a  

^a Department of Gastroenterology Hepatology and Nutrition ^*  (United States)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c MAIMONIDES MEDICAL CENTER   (United States)

Author keywords

Association; Crohn disease; Gene; Inflammatory bowel disease; Single nucleotide polymorphism

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15;

ADULT; ARTICLE; CHILD; CONTROLLED STUDY; CROHN DISEASE; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; IBD5 GENE; INFANT; JEW; MAJOR CLINICAL STUDY; MALE; OCTN1 GENE; OCTN2 GENE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

CHILD; CHROMOSOMES, HUMAN, PAIR 5; CROHN DISEASE; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; JEWS; LINKAGE DISEQUILIBRIUM; MALE; NOD2 SIGNALING ADAPTOR PROTEIN; ORGANIC CATION TRANSPORT PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; RAB GTP-BINDING PROTEINS;

EID: 67650901980     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPG.0b013e318183138a     Document Type: Article

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