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Volumn 16, Issue 14, 2010, Pages 1753-1758

NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease

Author keywords

ATG16L1; Childhood onset; Crohn's disease; Genetic susceptibility; Genetics; IL23R; Inflammatory bowel disease; NOD2 CARD15; Polymorphisms

Indexed keywords

AUTOPHAGY PROTEIN 5; AUTOPHAGY RELATED 16 LIKE 1 PROTEIN; CASPASE RECRUITMENT DOMAIN PROTEIN 15; INTERLEUKIN 23 RECEPTOR; UNCLASSIFIED DRUG;

EID: 77950995288     PISSN: 10079327     EISSN: None     Source Type: Journal    
DOI: 10.3748/wjg.v16.i14.1753     Document Type: Article
Times cited : (46)

References (35)
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  • 29
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    • NOD2/ CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease
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    • (2003) Am J Gastroenterol , vol.98 , pp. 2479-2484
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    • Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients
    • Yamazaki K, Onouchi Y, Takazoe M, Kubo M, Nakamura Y, Hata A. Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients. J Hum Genet 2007; 52: 575-583.
    • (2007) J Hum Genet , vol.52 , pp. 575-583
    • Yamazaki, K.1    Onouchi, Y.2    Takazoe, M.3    Kubo, M.4    Nakamura, Y.5    Hata, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.