Lack of common NOD2 mutations in Korean pediatric patients with inflammatory bowel disease

Pediatrics International

Volumn 52, Issue 6, 2010, Pages 888-889

  Jang, Joo Y ^a,b   Song, Seung M ^a   Kim, Kyung M ^a   Oh, Seak H ^a   Lee, Yeoun J ^a   Rhee, Kang W ^a  

^a University of Ulsan College of Medicine   (South Korea)

^b Ajou University School of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CROHN DISEASE; FEMALE; GENE MUTATION; HUMAN; KOREA; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; ULCERATIVE COLITIS;

ADOLESCENT; ALLELES; CHILD; COLITIS, ULCERATIVE; CROHN DISEASE; CROSS-CULTURAL COMPARISON; CROSS-SECTIONAL STUDIES; DNA MUTATIONAL ANALYSIS; FEMALE; GENE FREQUENCY; GENETIC VARIATION; HUMANS; INCIDENCE; KOREA; MALE; NOD2 SIGNALING ADAPTOR PROTEIN; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC;

EID: 78650480324     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2010.03269.x     Document Type: Article

References (10)

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