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

Pediatr Int. 2010 Dec;52(6):888-9. doi: 10.1111/j.1442-200X.2010.03269.x.

Authors

Joo Y Jang¹, Seung M Song, Kyung M Kim, Seak H Oh, Yeoun J Lee, Kang W Rhee

Affiliation

¹ Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

PMID: 21040192
DOI: 10.1111/j.1442-200X.2010.03269.x

No abstract available

Publication types

Comparative Study
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Alleles*
Child
Colitis, Ulcerative / epidemiology
Colitis, Ulcerative / ethnology
Colitis, Ulcerative / genetics*
Crohn Disease / epidemiology
Crohn Disease / ethnology
Crohn Disease / genetics*
Cross-Cultural Comparison*
Cross-Sectional Studies
DNA Mutational Analysis*
Female
Gene Frequency / genetics
Genetic Variation / genetics
Humans
Incidence
Korea
Male
Nod2 Signaling Adaptor Protein / genetics*
Polymerase Chain Reaction
Polymorphism, Genetic / genetics*

Substances

NOD2 protein, human
Nod2 Signaling Adaptor Protein