Infantile Onset Intractable Inflammatory Bowel Disease Due to Novel Heterozygous Mutations in TNFAIP3 (A20)
Author:
Affiliation:
1. Department of Gastroenterology, Pediatric Inflammatory Bowel Disease Research Center, Children’s Hospital of Fudan University, Shanghai, China
2. Department of Radiology, Children’s Hospital of Fudan University, Shanghai, China
Funder
National Natural Science Foundation of China
Publisher
Oxford University Press (OUP)
Subject
Gastroenterology,Immunology and Allergy
Link
http://academic.oup.com/ibdjournal/article-pdf/24/12/2613/26864130/izy165.pdf
Reference37 articles.
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2. Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification;Levine;Inflamm Bowel Dis,2011
3. Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia;Gonzaga-Jauregui;J Pediatr Gastroenterol Nutr,2014
4. Defective innate immunity in inflammatory bowel disease: a Crohn’s disease exclusivity;Marks;Curr Opin Gastroenterol,2011
5. Very early-onset inflammatory bowel disease: gaining insight through focused discovery;Moran;Inflamm Bowel Dis,2015
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