Frequent HPRT mutations in paroxysmal nocturnal haemoglobinuria reflect T cell clonal expansion, not genomic instability. [electronic resource]
Producer: 20040604Description: 383-91 p. digitalISSN:- 0007-1048
- Adult
- Cells, Cultured
- Colony-Forming Units Assay
- Complementarity Determining Regions -- metabolism
- Female
- Genomic Instability -- genetics
- Glycosylphosphatidylinositols -- blood
- Hemoglobinuria, Paroxysmal -- genetics
- Humans
- Hypoxanthine Phosphoribosyltransferase -- genetics
- Immunophenotyping
- Male
- Middle Aged
- Mutation
- Receptors, Antigen, T-Cell, alpha-beta -- genetics
- T-Lymphocyte Subsets -- drug effects
- Thioguanine -- pharmacology
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Publication Type: Journal Article
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