Role of phosphatidylinositol-linked proteins in paroxysmal nocturnal hemoglobinuria pathogenesis

Annual Review of Medicine

Volumn 47, Issue , 1996, Pages 1-10

  Kinoshita, Taroh ^a   Inoue, Norimitsu ^a   Takeda, Junji ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Complement; Hemolytic anemia; Somatic mutation

Indexed keywords

COMPLEMENT; GLYCOSYLPHOSPHATIDYLINOSITOL; MUTAGENIC AGENT; PHOSPHATIDYLINOSITOL; PROTEIN;

CELL CLONE; ERYTHROCYTE; GEOGRAPHIC DISTRIBUTION; HEMATOPOIETIC STEM CELL; HEMOLYTIC ANEMIA; HUMAN; LIPOGENESIS; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOGENESIS; PRIORITY JOURNAL; PROGENY; REVIEW; SOMATIC MUTATION;

ERYTHROCYTES; GLYCOSYLPHOSPHATIDYLINOSITOLS; HEMATOPOIETIC STEM CELLS; HEMOGLOBINURIA, PAROXYSMAL; HEMOLYSIS; HUMANS; LINKAGE (GENETICS); MEMBRANE PROTEINS; MUTATION; PHOSPHATIDYLINOSITOLS; SEX CHROMOSOME ABERRATIONS; X CHROMOSOME;

EID: 0029936421     PISSN: 00664219     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.med.47.1.1     Document Type: Review

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