Defective IL7R expression in T-B+NK+ severe combined immunodeficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng1298_394.pdf
Reference29 articles.
1. Leonard, W.J. The molecular basis of X-linked severe combined immunodeficiency: defective cytokine receptor signaling. Annu. Rev. Med. 47, 229–239 (1996).
2. Fischer, A. et al. Naturally occurring primary deficiencies of the immune system. Annu. Rev. Immunol. 15, 93– 124 (1997).
3. Buckley, R.H. et al. Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in 108 infants. J. Pediatr. 130, 378–387 (1997).
4. Noguchi, M. et al. Interleukin-2 receptor γ chain mutation results in X-linked severe combined immunodeficiency in humans. Cell 73, 147–157 (1993).
5. Kondo, M. et al. Sharing of the interleukin-2 (IL-2) receptor γ chain between receptors for IL-2 and IL-4. Science 262, 1874–1877 (1993).
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