The pathophysiology of paroxysmal nocturnal hemoglobinuria
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology
Reference93 articles.
1. The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis;Miyata;Science,1993
2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria;Takeda;Cell,1993
3. Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria;Miyata;N Engl J Med,1994
4. Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor;Nicholson-Weller;Proc Natl Acad Sci U S A,1983
5. Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria;Pangburn;Proc Natl Acad Sci U S A,1983
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