Identification of GFI1 mutations in adult patients with congenital neutropenia
Author:
Funder
European Cooperation in Science and Technology
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-022-04977-7.pdf
Reference10 articles.
1. Palmblad J, Dufour C, Papadaki HA (2014) How we diagnose neutropenia in the adult and elderly patient. Haematologica 99(7):1130–1133. https://doi.org/10.3324/haematol.2014.110288
2. Furutani E, Newburger PE, Shimamura A (2019) Neutropenia in the age of genetic testing: advances and challenges. Am J Hematol 94(3):384–393. https://doi.org/10.1002/ajh.25374
3. Dale DC, Bolyard AA, Steele LA, Zeidler C, Welte K (2020) Registries for study of nonmalignant hematological diseases: The example of the Severe Chronic Neutropenia International Registry. Curr Opin Hematol 27(1):18–26. https://doi.org/10.1097/MOH.0000000000000558
4. Richard E, Person RE, Li FQ, Duan Z et al (2003) Mutations in proto-oncogene GFI1 cause human neutropenia and target ELA2. Nat Genet 34(3):308–312. https://doi.org/10.1038/ng1170
5. Skokowa J, Dale DC, Touw IP, Zeidler C, Welte K (2017) Severe congenital neutropenias. Nat Rev Dis Primers 3:17032. https://doi.org/10.1038/nrdp.2017.32
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1. Neutropenia in Pediatric Oncological Patients;New Updates in Tumor Microenvironment [Working Title];2024-04-22
2. The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action;HemaSphere;2023-03-30
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