Molecular Genetics of Paroxysmal Nocturnal Hemoglobinuria
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/BF02983208/fulltext.html
Reference36 articles.
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2. Takeda J, Miyata T, Kawagoe K, 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. Rosse WE. New insights into paroxysmal nocturnal hemoglobinuria.Curr Opin Hematol. 2001:8:61–67.
4. Kinoshita T, Inoue N. Relationship between aplastic anemia and paroxysmal nocturnal hemoglobinuria.Int J Hematol. 2002;75:117–122.
5. Watanabe R, Murakami Y, Marmor MD, et al. Initial enzyme for glycosylphosphatidylinositol biosynthesis requires PIG-P and is regulated by DPM2.EMBO J. 2000;19:4402–4411.
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