Genetic defects in common variable immunodeficiency

International Journal of Immunogenetics

Volumn 34, Issue 4, 2007, Pages 225-229

  Kopecky O ^a   Lukesova S ^a  

^a UNIVERSITY HOSPITAL HRADEC KRALOVE   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

CD19 ANTIGEN; CD27 ANTIGEN; GENE PRODUCT; IMMUNOGLOBULIN M; INDUCIBLE COSTIMULATOR PROTEIN; INTERLEUKIN 10; INTERLEUKIN 13; INTERLEUKIN 2; INTERLEUKIN 4; INTERLEUKIN 5; TRANSMEMBRANE ACTIVATOR AND CALCIUM MODULATOR AND CYTOPHILIN LIGAND INTERACTOR PROTEIN; UNCLASSIFIED DRUG;

AUTOSOMAL RECESSIVE DISORDER; B LYMPHOCYTE; BACTERIAL INFECTION; CHROMOSOME 21; CHROMOSOME 6; CLINICAL FEATURE; COMMON VARIABLE IMMUNODEFICIENCY; GENE DELETION; GENE FUNCTION; GENETIC DISORDER; HUMAN; HYPOGAMMAGLOBULINEMIA; IMMUNOPATHOGENESIS; PRIORITY JOURNAL; REINFECTION; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; T LYMPHOCYTE ACTIVATION; TH2 CELL;

ANIMALS; COMMON VARIABLE IMMUNODEFICIENCY; HUMANS;

EID: 34447307933     PISSN: 17443121     EISSN: 1744313X     Source Type: Journal    
DOI: 10.1111/j.1744-313X.2007.00681.x     Document Type: Review

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