Paroxysmal nocturnal hemoglobinuria induced by the occurrence of BCR-ABL in a PIGA mutant hematopoietic progenitor cell
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
http://www.nature.com/articles/leu2015268.pdf
Reference15 articles.
1. Lewis SM, Dacie JV . The aplastic anaemia—paroxysmal nocturnal haemoglobinuria syndrome. Br J Haematol 1967; 13: 236–251.
2. Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y, Fujita T et al. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal-nocturnal hemoglobinuria. Cell 1993; 73: 703–711.
3. Ware RE, Rosse WF, Howard TA . Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria. Blood 1994; 83: 2418–2422.
4. Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV . Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995; 333: 1253–1258.
5. Inoue N, Izui-Sarumaru T, Murakami Y, Endo Y, Nishimura JI, Kurokawa K et al. Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH). Blood 2006; 108: 4232–4236.
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