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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
- Published in:
- Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
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- Article
Activation of autoreactive T-lymphocytes by cultured syngeneic glomerular mesangial cells.
- Published in:
- Kidney International, 1994, v. 45, n. 3, p. 763, doi. 10.1038/ki.1994.101
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- Publication type:
- Article