Haemophagocytic lymphohistiocytosis in X-linked severe combined immunodeficiency

British Journal of Haematology

Volumn 108, Issue 4, 2000, Pages 834-837

  Grunebaum, E ^b   Zhang, J ^b   Dadi, H ^b   Roifman, C M ^a  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

^b NONE

Author keywords

Haemophagocytic lymphohistiocytosis; IL 2 receptor , , common chain; Natural killer cells; Severe combined immune deficiency

Indexed keywords

INTERLEUKIN 2 RECEPTOR; RECEPTOR SUBUNIT;

ARTICLE; CASE REPORT; CLINICAL FEATURE; COMBINED IMMUNODEFICIENCY; ERYTHROPHAGOCYTOSIS; FLOW CYTOMETRY; GENE MUTATION; GENOTYPE; HISTIOCYTOSIS; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOPHENOTYPING; INFANT; MALE; NATURAL KILLER CELL; PRIORITY JOURNAL; T LYMPHOCYTE; X CHROMOSOME LINKED DISORDER;

BLOTTING, WESTERN; CELL LINE, TRANSFORMED; FLOW CYTOMETRY; HISTIOCYTOSIS, NON-LANGERHANS-CELL; HUMANS; INFANT; LINKAGE (GENETICS); MALE; POINT MUTATION; RECEPTORS, INTERLEUKIN-2; SEVERE COMBINED IMMUNODEFICIENCY; X CHROMOSOME;

EID: 0005837889     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2000.01923.x     Document Type: Article

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