TACI variants as underlying condition in autoimmune neutropenia: Description of four cases
Author:
Affiliation:
1. Hematology Unit–IRCCS Istituto Giannina Gaslini Genoa Italy
2. UOSD Genetics and Genomics of Rare Diseases IRCCS Istituto Giannina Gaslini Genoa Italy
3. Laboratory of Human Genetics–IRCCS Istituto Giannina Gaslini Genoa Italy
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26625
Reference11 articles.
1. Mutation in the TACI gene and autoimmune neutropenia: A case report
2. TACI deficiency — a complex system out of balance
3. Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
4. Primary immune regulatory disorders and targeted therapies;Kolukısa B;Turk J Haematol,2021
5. Treatment of immune-mediated cytopenias in patients with primary immunodeficiencies and immune regulatory disorders (PIRDs)
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1. Late‐onset and long‐lasting neutropenias in the young: A new entity anticipating immune‐dysregulation disorders;American Journal of Hematology;2024-01-29
2. A high prevalence of neutrophil‐specific antibodies in ELANE‐mutated severe congenital neutropenia;Pediatric Blood & Cancer;2023-02-03
3. Autoimmune Neutropenia and Immune-Dysregulation in a Patient Carrying a TINF2 Variant;International Journal of Molecular Sciences;2022-11-22
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