Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217-Reference-Cited by-同舟云学术

Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217

Published:2016-02-22 Issue:17 Volume:37 Page:1384-1394
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:Eur Heart J

Author:

Benn Marianne,Watts Gerald F.,Tybjærg-Hansen Anne,Nordestgaard Børge G.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/37/17/1384/17356328/ehw028.pdf

Reference38 articles.

1. Familial Hypercholesterolemia and Coronary Heart Disease: A HuGE Association Review

2. Goldstein JK , Hobbs HH , Brown MS . Familial hypercholesterolemia. In: Scriver CR , Beaudet AL , Sly WS , Valle D , eds. The Metabolic and Molecular Bases of Inherited Disease . 8th ed. New York: McGraw-Hill; 2001. p2863–2913.

3. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society

4. Genetic Causes of Monogenic Heterozygous Familial Hypercholesterolemia: A HuGE Prevalence Review

5. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society

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