PTPN22 gene polymorphism as a genetic risk factor for primary immune thrombocytopenia in Egyptian children
Author:
Affiliation:
1. Pediatric Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt
2. Medical Biochemistry Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt
Publisher
Informa UK Limited
Subject
Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/17474086.2020.1838895
Reference14 articles.
1. Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group
2. The Centenary of Immune Thrombocytopenia – Part 1: Revising Nomenclature and Pathogenesis
3. Impact of serum immunoglobulins level and IL-18 promoter gene polymorphism among Egyptian patients with idiopathic thrombocytopenic purpura
4. The role of PTPN22 gene polymorphism in childhood immune thrombocytopenic purpura
5. The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans
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1. Frequency of toll‐like receptor 4 variants and association with treatment response in children with primary immune thrombocytopenia;Pediatric Blood & Cancer;2023-08-28
2. Deciphering the genetic basis of immune thrombocytopenia: current evidence for genetic predisposition in adult ITP;Blood Advances;2023-07-18
3. Association of PTPN22 SNP1858 (rs2476601) and Gene SNP1123 (rs2488457) Polymorphism With Primary Immune Thrombocytopenia Susceptibility: A Meta-Analysis of Case-Control Studies and Trial Sequential Analysis;Frontiers in Genetics;2022-05-25
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