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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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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article

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wetenschappelijk artikel

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наукова стаття, опублікована в березні 2017

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A genetic database and clinica ...... r A and IL-10 Receptor B genes

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A genetic database and clinica ...... r A and IL-10 Receptor B genes

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A genetic database and clinica ...... r A and IL-10 Receptor B genes

@en

A genetic database and clinica ...... r A and IL-10 Receptor B genes

@nl

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A genetic database and clinica ...... r A and IL-10 Receptor B genes

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A genetic database and clinica ...... r A and IL-10 Receptor B genes

@nl

P1476

A genetic database and clinica ...... r A and IL-10 Receptor B genes

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Amarilla Bernadett Mandola

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Amit Nahum

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Yotam Eshel

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P2860

Novel exonic mutation inducing aberrant splicing in the IL10RA gene and resulting in infantile-onset inflammatory bowel disease: a case report

Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.

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

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

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.

Very early onset inflammatory bowel disease associated with aberrant trafficking of IL-10R1 and cure by T cell replete haploidentical bone marrow transplantation.

A Mendelian predisposition to B-cell lymphoma caused by IL-10R deficiency.

Very early-onset inflammatory bowel disease (IBD) in infancy is a different disease entity from adult-onset IBD; one form of interleukin-10 receptor mutations.

Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantation.

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

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scholarly article

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10.14785/LYMPHOSIGN-2016-0014

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2017-03-20T00:00:00Z

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P921

interleukin