Identification of the mutation responsible for a case of plasmatic apolipoprotein CII deficiency (Apo CII-bari)
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference21 articles.
1. A specific apoprotein activator for lipoprotein lipase
2. Inheritance of Apolipoprotein C-II Deficiency with Hypertriglyceridemia and Pancreatitis
3. Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients.
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3. Update on the molecular biology of dyslipidemias;Clinica Chimica Acta;2016-02
4. A novel APOC2 gene mutation identified in a Chinese patient with severe hypertriglyceridemia and recurrent pancreatitis;Lipids in Health and Disease;2016-01-16
5. Human genetics of HDL: Insight into particle metabolism and function;Progress in Lipid Research;2015-04
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