Inherited disorders of IL-12- and IFNγ-mediated immunity: a molecular genetics update
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Immunology
Reference38 articles.
1. Mycobacterium fortuitum–chelonae complex infection in a child with complete interleukin-12 receptor beta1 deficiency;Aksu;Pediatr. Infect. Dis. J.,2001
2. A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency;Allende;Clin. Diagn. Lab. Immunol.,2001
3. Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency;Altare;Science,1998
4. A causative relationship between mutant IFNγR1 alleles and impaired cellular response to IFNγ in a compound heterozygous child;Altare;Am. J. Hum. Genet.,1998
5. Inherited interleukin-12 deficiency in a child with bacille Calmette-Guerin and Salmonella enteritidis disseminated infection;Altare;J. Clin. Invest.,1998
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