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Properdin deficiency: molecular basis and disease association.
Fijen CA, van den Bogaard R, Schipper M, Mannens M, Schlesinger M, Nordin FG, Dankert J, Daha MR, Sjöholm AG, Truedsson L, Kuijper EJ. Fijen CA, et al. Among authors: kuijper ej. Mol Immunol. 1999 Sep-Oct;36(13-14):863-7. doi: 10.1016/s0161-5890(99)00107-8. Mol Immunol. 1999. PMID: 10698340 Review. No abstract available.
Heterozygous and homozygous factor H deficiency states in a Dutch family.
Fijen CA, Kuijper EJ, Te Bulte M, van de Heuvel MM, Holdrinet AC, Sim RB, Daha MR, Dankert J. Fijen CA, et al. Among authors: kuijper ej. Clin Exp Immunol. 1996 Sep;105(3):511-6. doi: 10.1046/j.1365-2249.1996.d01-777.x. Clin Exp Immunol. 1996. PMID: 8809142 Free PMC article.
482 results