Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference10 articles.
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2. Paroxysmal nocturnal haemoglobinuria: evidence of monoclonal origin of abnormal red cells;Oni;Blood,1970
3. Affected paroxysmal nocturnal haemoglobinuria T lymphocytes harbour a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A thy-1-murine lymphoma mutants;Armstrong;J Biol Chem,1992
4. The cloning of PIG-A, a component in the early step of GPI-anchor synthesis;Miyata;Science,1993
5. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal haemoglobinuria;Takeda;Cell,1993
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