Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia

Blood

Volumn 89, Issue 7, 1997, Pages 2369-2375

  Tidow, N ^a   Pilz, C ^a   Teichmann, B ^a   Muller Brechlin A ^a   Germeshausen, M ^a   Kasper, B ^a   Rauprich, P ^a   Sykora, K W ^a   Welte, K ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COLONY STIMULATING FACTOR RECEPTOR; COMPLEMENTARY DNA; GRANULOCYTE COLONY STIMULATING FACTOR; RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR;

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; ARTICLE; BLOOD ANALYSIS; BONE MARROW CELL; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL TRIAL; DNA DETERMINATION; DNA SEQUENCE; HUMAN; HUMAN CELL; LEUKEMOGENESIS; NEUTROPENIA; PEDIGREE; PHASE 1 CLINICAL TRIAL; PHASE 2 CLINICAL TRIAL; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECEPTOR GENE; RNA ANALYSIS;

EID: 0030945921     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v89.7.2369     Document Type: Article

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