Translational Mini-Review Series on Immunodeficiency: Molecular defects in common variable immunodeficiency
Author:
Affiliation:
1. Molecular Immunology Unit, Institute of Child Health, London, UK
2. Department of Clinical Immunology, Great Ormond Street Hospital, London, UK
Abstract
Publisher
Oxford University Press (OUP)
Subject
Immunology,Immunology and Allergy
Link
https://academic.oup.com/cei/article-pdf/149/3/401/42037996/j.1365-2249.2007.03461.x.pdf
Reference60 articles.
1. Physiology of Iga and Iga deficiency;Cunningham-Rundles;J Clin Immunol,2001
2. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies);Conley;Clin Immunol,1999
3. Common variable immunodeficiency: clinical and immunological features of 248 patients;Cunningham-Rundles;Clin Immunol,1999
4. Common variable immunodeficiency: a review;Di Renzo;Clin Exp Med,2004
5. Severe deficiency of switched memory B cells (CD27(+) IgM(-) IgD(-) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease;Warnatz;Blood,2002
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