Impact of a common mutation of the LDL receptor gene, in French-Canadian patients with familial hypercholesterolemia, on means, variances and correlations among traits of lipid metabolism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb03925.x/fullpdf
Reference36 articles.
1. Joint distribution of lipoprotein cholesterol classes;Abbott;Arteriosclerosis,1983
2. Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians;Bétard;Hum Genet,1992
3. The role of apoproteins in disorders of lipoprotein metabolism;Frohlich;Clin Biochem,1989
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1. Spectrum of low-density lipoprotein receptor (LDLR) mutations in a cohort of Sri Lankan patients with familial hypercholesterolemia – a preliminary report;Lipids in Health and Disease;2018-05-02
2. Role of rs3846662 and HMGCR alternative splicing in statin efficacy and baseline lipid levels in familial hypercholesterolemia;Pharmacogenetics and Genomics;2016-01
3. A novel point mutation (Pro84 ← Ser) of the low density lipoprotein receptor gene in a family with moderate hypercholesterolemia;Clinical Genetics;2008-06-28
4. Heritability of Longitudinal Changes in Coronary-Heart-Disease Risk Factors in Women Twins;The American Journal of Human Genetics;1997-06
5. Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-receptor gene defect;Atherosclerosis;1996-01
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