DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03135.x/fullpdf
Reference14 articles.
1. Deletion in the gene for the low-density lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia;Hobbs;N Engl J Med,1987
2. Evidence for a dominant gene that suppresses hypercholesterolemia in a family with defective low density lipoprotein receptors;Hobbs;J Clin Invest,1989
3. The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein;Hobbs;Ann Rev Genet,1990
4. A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis;Humphries;Lancet,1985
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1. Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart disease;Clinical Genetics;2008-06-28
2. Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa;Clinical Genetics;2008-04-23
3. Intrafamilial variability in the clinical expression of familial hypercholesterolemia: importance of risk factor determination for genetic counselling;Clinical Genetics;2008-04-23
4. Simultaneous Detection of Multiple Familial Hypercholesterolemia Mutations Facilitates an Improved Diagnostic Service in South African Patients at High Risk of Cardiovascular Disease;Molecular Diagnosis;2003-09
5. Low-density lipoprotein receptor gene mutation analysis and clinical correlation in Belgian hypercholesterolaemics;Molecular and Cellular Probes;2001-12
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