Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase —No detection by newborn screening for primary immunodeficiencies-Reference-Cited by-同舟云学术

Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase —No detection by newborn screening for primary immunodeficiencies

Published:2019-10-30 Issue:1 Volume:91 Page:
ISSN:0300-9475
Container-title:Scandinavian Journal of Immunology
language:en
Short-container-title:Scand J Immunol

Author:

Krüger Renate¹^ORCID,Baumann Ulrich²,Borte Stephan³,Kölsch Uwe⁴,Lorenz Myriam Ricarda⁵,Keller Baerbel⁶⁷,Harder Ina⁶⁷,Warnatz Klaus⁶⁷,Ehl Stephan⁷,Schwarz Klaus⁵,Wahn Volker¹,Bernuth Horst¹⁴⁸

Affiliation:

1. Department of Pediatric Pneumology, Immunology and Intensive Care, Charité–Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin Humboldt‐Universität zu Berlin and Berlin Institute of Health Berlin Germany

2. Department of Pediatric Pulmonology Hannover Medical School Hannover Germany

3. ImmunoDeficiencyCenter Leipzig (IDCL), Jeffrey Modell Diagnostic and Research Center for Primary Immunodeficiencies Municipal Hospital St. Georg Leipzig Germany

4. Department of Immunology Labor Berlin - Charité Vivantes GmbH Berlin Germany

5. Institute for Transfusion Medicine, German Red Cross Blood Service Baden‐Wuerttemberg–Hessen University Ulm and Institute for Clinical Transfusion Medicine and Immunogenetics Ulm Ulm Germany

6. Department of Rheumatology and Clinical Immunology, Faculty of Medicine, Medical Center‐University of Freiburg University of Freiburg Freiburg Germany

7. Center for Chronic Immunodeficiency, Faculty of Medicine, Medical Center‐University of Freiburg University of Freiburg Freiburg Germany

8. Berlin Center for Regenerative Therapies (BCRT) Charité‐Universitätsmedizin Berlin Germany

Publisher

Wiley

Subject

Immunology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/sji.12811

Reference28 articles.

1. Agammaglobulinemia;Bruton OC;Pediatrics,1952

2. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

3. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases