Haplotype analysis at the low density lipoprotein receptor locus in normal and familial hypercholesterolemia Norwegian subjects
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03883.x/fullpdf
Reference24 articles.
1. Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype;Aalto-Setälä;J Clin Invest,1989
2. Haplotype analysis at the low density lipoprotein receptor locus: application to the study of familial hyperchol-esterolemia in Israel;Berkman;Hum Genet,1992
3. PstI RFLP close to the LDL receptor gene;Funke;Nucleic Acids Res,1986
4. Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia;Goldstein;J Clin Invest,1973
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1. Seven DNA polymorphisms in the LDL receptor gene: application to the study of familial hypercholesterolemia in Spain;Clinical Genetics;2008-06-28
2. Familial hypercholesterolemia study in Sardinia using 6 LDLR polymorphic markers based on PCR;American Journal of Medical Genetics;2000-03-06
3. The genetic algorithm applied to haplotype data at the LDL receptor locus;Computer Methods and Programs in Biomedicine;2000-01
4. Phenotypic consequences of a deletion of exons 2 and 3 of the LDL receptor gene;Journal of Lipid Research;1999-02
5. Mutant transcripts of the LDL receptor gene: mRNA structure and quantity;Human Mutation;1999
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