Defects of leukocyte migration in primary immunodeficiencies
Author:
Affiliation:
1. Department of Pediatrics; Institute of Molecular Medicine “Angelo Nocivelli”, University of Brescia, Brescia; Italy
Publisher
Wiley
Subject
Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/eji.201243155/fullpdf
Reference63 articles.
1. Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease
2. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome
3. WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12
4. Clinical and Genetic Features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) Syndrome
5. Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry
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