A compound heterozygote for lipoprotein lipase deficiency, Val69–>Leu and Gly188–>Glu: correlation between in vitro LPL activity and clinical expression.

by T. Bruin, S. Tuzgöl, W.J. Mulder, A.E. van den Ende, H. Jansen, M.R. Hayden, J.J. Kastelein
Published 1994-03-01

Mutations in the low density lipoprotein receptor gene of familial hypercholesterolemic patients detected by denaturing gradient gel electrophoresis and direct sequencing.

by P Lombardi, E J Sijbrands, K van de Giessen, A H Smelt, J J Kastelein, R R Frants, L M Havekes
Published 1995-04-01

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

by 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
Published 1996-03-01

Lipoprotein[a] is not present in the plasma of patients with some peroxisomal disorders

by Y Y van der Hoek, R J Wanders, A E van den Ende, H G Kraft, B R Gabel, J J Kastelein, M L Koschinsky
Published 1997-08-01