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Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.
Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J, Vigneau C, Kuypers D, Boudailliez B, Loirat C, Rondeau E, Fridman WH. Fremeaux-Bacchi V, et al. Among authors: fridman wh. J Med Genet. 2004 Jun;41(6):e84. doi: 10.1136/jmg.2004.019083. J Med Genet. 2004. PMID: 15173250 Free PMC article. No abstract available.
Restricted genetic defects underlie human complement C6 deficiency.
Dragon-Durey MA, Fremeaux-Bacchi V, Blouin J, Barraud D, Fridman WH, Kazatchkine MD. Dragon-Durey MA, et al. Among authors: fridman wh. Clin Exp Immunol. 2003 Apr;132(1):87-91. doi: 10.1046/j.1365-2249.2003.02099.x. Clin Exp Immunol. 2003. PMID: 12653841 Free PMC article.
536 results