PTPN22 gene polymorphism as a genetic risk factor for primary immune thrombocytopenia in Egyptian children.

Conclusion: PTPN22 gene polymorphism may play a pivotal role in genetic predisposition to ITP and disease progress in Egyptian children.
PMID: 33064968 [PubMed - as supplied by publisher]

Source: Expert Review of Hematology - October 20, 2020 Category: Hematology Tags: Expert Rev Hematol Source Type: research