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28. Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations. Sessa A; Battini G; Meroni M; Daidone G; Carnera I; Brambilla PL; Viganò G; Giordano F; Pallotti F; Torri Tarelli L; Calabresi L; Rolleri M; Bertolini S Nephron; 2001 Jul; 88(3):268-72. PubMed ID: 11423760 [TBL] [Abstract][Full Text] [Related]
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31. Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: lipid composition and reactivity in vitro. Glomset JA; Norum KR; King W J Clin Invest; 1970 Oct; 49(10):1827-37. PubMed ID: 5456796 [TBL] [Abstract][Full Text] [Related]
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