High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Cancer Research,Hematology
Link
http://www.nature.com/articles/2404135.pdf
Reference34 articles.
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2. Miyata T, Takeda J, Iida Y, Yamada N, Inoue N, Takahashi M et al. The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 1993; 259: 1318–1320.
3. Shichishima T, Noji H . A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria. Hematology 2002; 7: 211–227.
4. Young NS . The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated. Blood 1992; 79: 1385–1392.
5. Schubert J, Vogt HG, Zielinska-Skowronek M, Freund M, Kaltwasser JP, Hoelzer D et al. Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood 1994; 83: 2323–2328.
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