Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia-Reference-Cited by-同舟云学术

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia

Published:2014-07-24 Issue:4 Volume:124 Page:655-657
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Serwas Nina Kathrin¹^ORCID,Cagdas Deniz²,Ban Sol A.¹,Bienemann Kirsten³,Salzer Elisabeth¹,Tezcan İlhan²,Borkhardt Arndt³,Sanal Ozden²,Boztug Kaan¹⁴

Affiliation:

1. CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria

2. Division of Immunology, Hacettepe University Ihsan Doğramacı Children’s Hospital, Ankara, Turkey

3. Department of Paediatric Oncology, Haematology and Clinical Immunology, Center for Child and Adolescent Health, Heinrich Heine University, Düsseldorf, Germany

4. Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/124/4/655/1382454/655.pdf

Reference11 articles.

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2. Idiopathic CD4+ T lymphopenia without autoimmunity or granulomatous disease in the slipstream of RAG mutations.;Kuijpers;Blood,2011

3. MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival.;Nehme;Blood,2012

4. Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency.;Salzer;J Allergy Clin Immunol,2014

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