Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease-Reference-Cited by-同舟云学术

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Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease

Published:2012-04-05 Issue:5 Volume:13 Page:437-442
ISSN:1466-4879
Container-title:Genes & Immunity
language:en
Short-container-title:Genes Immun

Author:

Mao H,Yang W,Lee P P W,Ho M H-K,Yang J,Zeng S,Chong C-Y,Lee T-L,Tu W,Lau Y-L

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Immunology

Link

http://www.nature.com/articles/gene20128.pdf

Reference25 articles.

1. Baumgart DC, Sandborn WJ . Inflammatory bowel disease: clinical aspects and established and evolving therapies. Lancet 2007; 369: 1641–1657.

2. Baumgart DC, Carding SR . Inflammatory bowel disease: cause and immunobiology. Lancet 2007; 369: 1627–1640.

3. Abraham C, Cho JH . Inflammatory bowel disease. N Engl J Med 2009; 361: 2066–2078.

4. Franke A, McGovern DP, Barrett JC, Wang K, Radford-Smith GL, Ahmad T et al. Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet 2010; 42: 1118–1125.

5. Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, Premkumar L et al. Whole-exome-sequencing-based discovery of human FADD deficiency. Am J Hum Genet 2010; 87: 873–881.

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