Impaired myelopoiesis in congenital neutropenia: insights into clonal and malignant hematopoiesis
Author:
Affiliation:
1. Division of Hematology-Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO
2. Division of Oncology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO
Abstract
Publisher
American Society of Hematology
Subject
Hematology
Link
https://ashpublications.org/hematology/article-pdf/2021/1/514/1851470/514warren.pdf
Reference50 articles.
1. Severe congenital neutropenias;Skokowa;Nat Rev Dis Primers,2017
2. A syndrome with congenital neutropenia and mutations in G6PC3;Boztug;N Engl J Med,2009
3. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesis;Horwitz;Nat Genet,1999
4. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease);Klein;Nat Genet,2007
5. Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia;Xia;Br J Haematol,2009
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