Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease. - Wikidata - awgldk - TriplyDB

Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.

Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.

http://www.wikidata.org/entity/Q37030211

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Mutations in Interleukin-10 Receptor and Clinical Phenotypes in Patients with Very Early Onset Inflammatory Bowel Disease: A Chinese VEO-IBD Collaboration Group Survey.IL-10 and IL-10 Receptor Mutations in Very Early Onset Inflammatory Bowel Disease.Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.Childhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene.Phenotypic and genotypic characterization of inflammatory bowel disease in children under six years of age in China.Study of disease phenotype and its association with prognosis of paediatric inflammatory bowel disease in China.A genetic database and clinical findings for immunodeficiency due to mutations in Interleukin -10, IL-10 Receptor A and IL-10 Receptor B genes

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Comprehensive mutation screening for 10 genes in Chinese patients suffering very early onset inflammatory bowel disease.

http://www.wikidata.org/entity/Q37030211

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Comprehensive mutation screeni ...... et inflammatory bowel disease.

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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type

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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WJG.V22.I24.5578

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World Journal of Gastroenterology

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Comprehensive mutation screeni ...... et inflammatory bowel disease.

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Chun-Di Xu

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Ling Gong

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Tong Zhou

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Xiao-Qin Li

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Xin-Qiong Wang

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Xu Xu

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Yan Guo

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Yi Yu

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Yuan Xiao

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P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Common variants at five new loci associated with early-onset inflammatory bowel disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

The diagnostic approach to monogenic very early onset inflammatory bowel disease

Interleukin-10-deficient mice develop chronic enterocolitis

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes

IL-10R polymorphisms are associated with very-early-onset ulcerative colitis.

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease

Synergistic effect of interleukin-10-receptor variants in a case of early-onset ulcerative colitis.

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5578-5588

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scholarly article

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10.3748/WJG.V22.I24.5578

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2016-06-01T00:00:00Z

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27350736

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Very early onset inflammatory bowel disease

inflammatory bowel diseases

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4917618

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