Functional analysis of new 3′ untranslated regions genetic variants in genes associated with genetic hypercholesterolemias-Reference-Cited by-同舟云学术

Functional analysis of new 3′ untranslated regions genetic variants in genes associated with genetic hypercholesterolemias

Published:2017-03 Issue:2 Volume:11 Page:532-542
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Pérez-Campo Flor María,De Castro-Orós Isabel,Noriega Alicia,Cofán Montserrat,Lamiquiz-Moneo Itziar,Cenarro Ana,Ros Emilio,Civeira Fernando,Pocoví Miguel,Rodríguez-Rey José Carlos

Funder

Spanish Ministry of Health

Instituto de Salud Carlos III

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference46 articles.

1. A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia;Marks;Atherosclerosis,2003

2. Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states;Slack;Lancet,1969

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;Nordestgaard;Eur Heart J,2013

4. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia;Abifadel;Nat Genet,2003

5. Guidelines for the diagnosis and management of heterozygous familial hypercholesterolemia;Civeira;Atherosclerosis,2004

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