Chen, Guibin <br/><br/>
Frequent HPRT mutations in paroxysmal nocturnal haemoglobinuria reflect T cell clonal expansion, not genomic instability.  [electronic resource] 

 -  British journal of haematology  May 2004 
 - 383-91 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.2004.04912.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Cells, Cultured<br/>Colony-Forming Units Assay<br/>Complementarity Determining Regions--metabolism<br/>Female<br/>Genomic Instability--genetics<br/>Glycosylphosphatidylinositols--blood<br/>Hemoglobinuria, Paroxysmal--genetics<br/>Humans<br/>Hypoxanthine Phosphoribosyltransferase--genetics<br/>Immunophenotyping<br/>Male<br/>Middle Aged<br/>Mutation<br/>Receptors, Antigen, T-Cell, alpha-beta--genetics<br/>T-Lymphocyte Subsets--drug effects<br/>Thioguanine--pharmacology