Familial hyperchylomicronemia
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference30 articles.
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1. The genetic architecture of the familial hyperlipidaemia syndromes;Current Opinion in Lipidology;2014-08
2. Detection and characterization of the heterozygote state for lipoprotein lipase deficiency.;Arteriosclerosis: An Official Journal of the American Heart Association, Inc.;1989-05
3. Dermal, subcutaneous, and tendon xanthomas: Diagnostic markers for specific lipoprotein disorders;Journal of the American Academy of Dermatology;1988-07
4. Lipoprotein metabolism during acute inhibition of lipoprotein lipase in the cynomolgus monkey.;Journal of Clinical Investigation;1988-02-01
5. Clearance defects in primary chylomicronemia: A study of tissue lipoprotein lipase activities;Metabolism;1986-11
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