Alterations in plasma lipoproteins and apolipoproteins before the age of 40 in heterozygotes for lipoprotein lipase deficiency

We have assessed the expression of heterozygosity for lipoprotein lipase (LPL) deficiency by studying a single large French Canadian family comprising 92 persons including 21 carriers of the catalytically defective P207L mutation. Phenotypic changes distinguishing heterozygotes from controls were se...

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Bibliographic Details
Main Authors: S Bijvoet, S E Gagné, S Moorjani, C Gagné, H E Henderson, J C Fruchart, J Dallongeville, P Alaupovic, M Prins, J J Kastelein, M R Hayden
Format: Article
Language:English
Published: Elsevier 1996-03-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520376057