Compound heterozygote of cholesteryl-ester transfer protein deficiency in a patient with hyperalphalipoproteinemia
- 30 September 1992
- journal article
- other
- Published by Elsevier in Atherosclerosis
- Vol. 96 (1) , 83-85
- https://doi.org/10.1016/0021-9150(92)90040-n
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene MutationNew England Journal of Medicine, 1990
- Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteinsNature, 1989
- Decreased serum cholesteryl-ester transfer activity in a patient with familial hyper-alpha-lipoproteinemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1988