Genomewide Scan for Familial Combined Hyperlipidemia Genes in Finnish Families, Suggesting Multiple Susceptibility Loci Influencing Triglyceride, Cholesterol, and Apolipoprotein B Levels
- 1 May 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (5) , 1453-1463
- https://doi.org/10.1086/302365
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- A Common Genetic Mechanism Determines Plasma Apolipoprotein B Levels and Dense LDL Subfraction Distribution in Familial Combined HyperlipidemiaAmerican Journal of Human Genetics, 1998
- Glucose intolerance in familial combined hyperlipidaemiaEuropean Journal of Clinical Investigation, 1998
- Phenotype expression in familial combined hyperlipidemiaAtherosclerosis, 1997
- Is familial combined hyperlipidaemia a genetic disorder of adipose tissue?Current Opinion in Lipidology, 1997
- ReviewBiological Chemistry Hoppe-Seyler, 1995
- Twenty-Year Trends in Coronary Risk Factors in North Karelia and in Other Areas of FinlandInternational Journal of Epidemiology, 1994
- Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21Science, 1990
- Identification of the 64K autoantigen in insulin-dependent diabetes as the GABA-synthesizing enzyme glutamic acid decarboxylaseNature, 1990
- Amino acid sequence of the human fibronectin receptor.The Journal of cell biology, 1987
- Detection of Familial Hypercholesterolemia by Assaying Functional Low-Density-Lipoprotein Receptors on LymphocytesNew England Journal of Medicine, 1986