Increased representation of the PTPN22 mutation in patients with immune thrombocytopenia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2010.03954.x/fullpdf
Reference19 articles.
1. Chronic immune thrombocytopenic purpura in monozygotic twins;Laster;N Engl J Med,1982
2. Familial association of autoimmune thrombocytopenia and hyperthyroidism;Bizzaro;Am J Hematol,1992
3. PTPN22: setting thresholds for autoimmunity;Gregersen;Semin Immunol,2006
4. Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE;Kyogoku;Am J Hum Genet,2004
5. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes;Bottini;Nat Genet,2004
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1. Deciphering the genetic basis of immune thrombocytopenia: current evidence for genetic predisposition in adult ITP;Blood Advances;2023-07-18
2. 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
3. PTPN22 gene polymorphism as a genetic risk factor for primary immune thrombocytopenia in Egyptian children;Expert Review of Hematology;2020-11-02
4. The potential of PTPN22 as a therapeutic target for rheumatoid arthritis;Expert Opinion on Therapeutic Targets;2018-09-25
5. Pathogenesis of immune thrombocytopenia;Autoimmunity Reviews;2017-06
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