Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a Chinese patient with hypertriglyceridemia-Reference-Cited by-同舟云学术

Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a Chinese patient with hypertriglyceridemia

Published:2000-01 Issue:1 Volume:30 Page:33-40
ISSN:0014-2972
Container-title:European Journal of Clinical Investigation
language:en
Short-container-title:European Journal of Clinical Investigation

Author:

Chan ,Mak ,Tomlinson ,Baum ,Wu ,Masarei ,Pang

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2362.2000.00587.x/fullpdf

Reference39 articles.

1. Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis

2. Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

3. Gene environment interaction and plasma triglyceride levels: the crucial role of lipoprotein lipase

4. 4 JD Brunzell . Familial lipoprotein lipase deficiency and other causes of the chylomicronaemia syndrome. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors.The Metabolic Basis of Inherited Disease. 6th ed. New York: McGraw-Hill; 1995 Cover month: January(2). p. 1913, 32 .

5. Structure, function and role of lipoprotein lipase in lipoprotein metabolism

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