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Journal of Clinical Immunology
Literature
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Walter JE, Rosen LB, Csomos K, et al. Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency. J Clin Invest. 2015;125:4135–48.CrossRefPubMed
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Price S, Shaw PA, Seitz A, et al. Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations. Blood. 2014;123:1989–99.CrossRefPubMedPubMedCentral
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Salzer U, Bacchelli C, Buckridge S, et al. Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. Blood. 2009;113:1967–76.CrossRefPubMedPubMedCentral
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Felgentreff K, Baxi SN, Lee YN, et al. Ligase-4 deficiency causes distinctive immune abnormalities in asymptomatic individuals. J Clin Immunol. 2016;36:341--353.
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Guo C, Nakazawa Y, Woodbine L, et al. XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency. J Allergy Clin Immunol. 2015;136:1007–17.CrossRefPubMed
Metadata
Title
The Evolving Landscape of Primary Immunodeficiencies
Author
Andrew R. Gennery
Publication date
01-05-2016
Publisher
Springer US
Published in
Journal of Clinical Immunology / Issue 4/2016
Print ISSN: 0271-9142
Electronic ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-016-0273-6

Other articles of this Issue 4/2016

Journal of Clinical Immunology 4/2016 Go to the issue

Letter to Editor

Myelodysplastic Syndrome and Acute Lymphocytic Leukemia in Common Variable Immunodeficiency (CVID)

CME Review

Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease

Letter to Editor

Presenting features and platelet anomalies in WAS: one centre’s experience

Original Article

WHIM Syndrome Caused by Waldenström’s Macroglobulinemia-Associated Mutation CXCR4 L329fs

Original Article

Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals

Erratum

Erratum to: Adenosine Deaminase Deficient Severe Combined Immunodeficiency Presenting as Atypical Haemolytic Uraemic Syndrome

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