Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 9, 1999, Pages 5209-5214

  Araten, David J ^a   Nafa, Khedoudja ^a   Pakdeesuwan, Kriangsak ^b   Luzzatto, Lucio ^a  

^a MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; FLOW CYTOMETRY; FRAMESHIFT MUTATION; GENETIC LINKAGE; GENOTYPE; HUMAN; HUMAN CELL; MALE; MISSENSE MUTATION; MOLECULAR CLONING; NONSENSE MUTATION; NORMAL HUMAN; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RISK ASSESSMENT;

ADULT; AGED; CLONE CELLS; FLOW CYTOMETRY; HEMATOPOIETIC STEM CELLS; HEMOGLOBINURIA, PAROXYSMAL; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; PHENOTYPE;

EID: 0033609114     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.9.5209     Document Type: Article

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