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Results: 1-3 |
Results: 3
The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia
Authors: Hoffer, MJV Snieder, H Bredie, SJH Demacker, PNM Kastelein, JJP Frants, RR Stalenhoef, AFH
Citation: Mjv. Hoffer et al., The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia, ATHEROSCLER, 151(2), 2000, pp. 443-450
Familial chylomicronemia caused by a novel type of mutation in the APOE-CI-CIV-CII gene cluster encompassing both the APOCII gene and the first APOCIV gene mutation: APOCII-CIVNijmegen
Authors: de Graaf, J Hoffer, MJV Stuyt, PMJ Frants, RR Stalenhoef, AFH
Citation: J. De Graaf et al., Familial chylomicronemia caused by a novel type of mutation in the APOE-CI-CIV-CII gene cluster encompassing both the APOCII gene and the first APOCIV gene mutation: APOCII-CIVNijmegen, BIOC BIOP R, 273(3), 2000, pp. 1084-1087
Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphism
Authors: Sijbrands, EJ Hoffer, MJV Meinders, AE Havekes, LM Frants, RR Smelt, AHM De Knijff, P
Citation: Ej. Sijbrands et al., Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphism, ART THROM V, 19(11), 1999, pp. 2722-2729
Risultati: 1-3 |