Metabolism of apoB-100-containing lipoproteins in familial hyperchylomicronemia.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference30 articles.
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3. Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene;Ameis;J. Clin. Invest.,1991
4. A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians;Ma;N. Engl. J. Med.,1991
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