The molecular basis of X-linked severe combined immunodeficiency: Defective cytokine receptor signaling

Annual Review of Medicine

Volumn 47, Issue , 1996, Pages 229-239

  Leonard, Warren J ^a  

^a NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

Author keywords

(c); Common chain; IL 2 receptor; Immunodeficiency; XSCID

Indexed keywords

CYTOKINE RECEPTOR; INTERLEUKIN 15; INTERLEUKIN 2; INTERLEUKIN 2 RECEPTOR; INTERLEUKIN 4; INTERLEUKIN 7; INTERLEUKIN 9;

CELLULAR IMMUNITY; CHROMOSOME XQ; CLINICAL FEATURE; COMBINED IMMUNODEFICIENCY; FEMALE; GENE MUTATION; GENE THERAPY; GENETIC DISORDER; HETEROZYGOTE; HUMAN; HUMORAL IMMUNITY; MALE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; T LYMPHOCYTE ACTIVATION; X CHROMOSOME LINKAGE;

ANIMALS; DNA MUTATIONAL ANALYSIS; FEMALE; GENE REARRANGEMENT, GAMMA-CHAIN T-CELL ANTIGEN RECEPTOR; HUMANS; INTERLEUKINS; LINKAGE (GENETICS); LYMPHOCYTE ACTIVATION; MALE; MICE; RECEPTORS, CYTOKINE; RECEPTORS, INTERLEUKIN; RECEPTORS, INTERLEUKIN-2; SEVERE COMBINED IMMUNODEFICIENCY; SEX CHROMOSOME ABERRATIONS; SIGNAL TRANSDUCTION; T-LYMPHOCYTES; X CHROMOSOME;

EID: 0029924265     PISSN: 00664219     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.med.47.1.229     Document Type: Review

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