Mutational landscape and its clinical significance in paroxysmal nocturnal hemoglobinuria
Author:
Funder
Natural Science Foundation of Beijing Municipality
Chinese Academy of Medical Sciences
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Hematology
Link
http://www.nature.com/articles/s41408-021-00451-1.pdf
Reference9 articles.
1. Hill, A., DeZern, A. E., Kinoshita, T. & Brodsky, R. A. Paroxysmal nocturnal haemoglobinuria. Nat. Rev. Dis. Primers. 3, 14 (2017).
2. de Latour, R. P. et al. Paroxysmal nocturnal hemoglobinuria: natural history of disease subcategories. Blood. 112, 3099–3106 (2008).
3. Yoshizato, T. et al. Somatic mutations and clonal hematopoiesis in aplastic anemia. N. Engl. J. Med. 373, 35–47 (2015).
4. Li, L. Y. et al. Deep sequencing of whole genome exon in paroxysmal nocturnal hemoglobinuria. Am J Hematol. 92, E51–E53 (2017).
5. Shen, W. et al. Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria. J. Clin. Investig. 124, 4529–4538 (2014).
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