Abnormal regulation of the LDL-R and HMG CoA reductase genes in subjects with familial hypercholesterolemia with the “French Canadian Mutation”
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference44 articles.
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5. Common low-density lipoprotein receptor mutations in the French Canadian population;Leitersdorf;J Clin Invest,1990
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4. Familial hypercholesterolemia. Acceptor splice site (G→C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-RHonduras-1 [LDL-R1061(−1) G→C];Atherosclerosis;1999-09
5. Cellular Cholesterol Transport and Efflux in Fibroblasts Are Abnormal in Subjects With Familial HDL Deficiency;Arteriosclerosis, Thrombosis, and Vascular Biology;1999-01
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