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Defective glycosyl phosphatidylinositol anchor synthesis and paroxysmal nocturnal hemoglobinuria
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The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
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Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
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Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia
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Analysis of PIG-a gene in a patient who developed reciprocal translocation of chromosome 12 and paroxysmal nocturnal hemoglobinuria during follow-up of aplastic anemia
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The molecular basis of paroxysmal nocturnal hemoglobinuria
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Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients
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Savoia, A., Ianzano, L., Lunardi, C., De Sandre, G., Carotenuto, M., Musto, P. & Zelante, L. (1996) Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients. Human Genetics, 97, 45-48.
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0027310539
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Deficiency of the GPI anchor caused by a somatic mutation of the PIG-a gene in paroxysmal nocturnal hemoglobinuria
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The novel monoclonal antibody By114 helps detect the early emergence of a paroxysmal nocturnal hemoglobinuria clone in aplastic anemia
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Tooze, J.A., Saso, R., Marsh, J.C., Papadopoulos, A., Pulford, K. & Gordon-Smith, E.C. (1995) The novel monoclonal antibody By114 helps detect the early emergence of a paroxysmal nocturnal hemoglobinuria clone in aplastic anemia. Experimental Hematology, 21, 1484-1491.
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Paroxysmal nocturnal hemoglobinuria and the glycosylphosphatidylinositol anchor
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Yeh, E.T.1
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