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-Reference-Cited by-同舟云学术

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

Published:1996-01 Issue:1 Volume:119 Page:43-55
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Bétard Christine,Kessling A.M.,Roy M.,Davignon J.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference49 articles.

1. Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French-Canadians;Bétard;Hum Genet,1992

2. Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3 methylglutaryl coenzyme A reductase activity;Brown,1974

3. Xanthomata, hypercholesterolemia, angina pectoris;Muller;Acta Med Scand Suppl,1938

4. The inheritance of essential familial hypercholesterolemia;Khachadurian;Ann J Med,1964

5. Familial hypercholesterolemia;Goldstein,1989

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Coronary Artery Disease in French Canadians—Investigation of a Suggested Vulnerable Population;Canadian Journal of Cardiology;2016-10

2. Role of rs3846662 and HMGCR alternative splicing in statin efficacy and baseline lipid levels in familial hypercholesterolemia;Pharmacogenetics and Genomics;2016-01

3. Diagnosis of families with familial hypercholesterolaemia and/or Apo B-100 defect by means of DNA analysis of LDL-receptor gene mutations;Journal of Inherited Metabolic Disease;2007-03-08

4. Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia;European Heart Journal;2007-01-11

5. Influence of LDL receptor gene mutations and the R3500Q mutation of the apoB gene on lipoprotein phenotype of familial hypercholesterolemic patients from a South European population;European Journal of Human Genetics;2003-09-24