Genetic testing for familial hypercholesterolaemia: utility beyond diagnosis-Reference-Cited by-同舟云学术

Genetic testing for familial hypercholesterolaemia: utility beyond diagnosis

Published:2022-11-10 Issue: Volume: Page:
ISSN:2047-4873
Container-title:European Journal of Preventive Cardiology
language:en
Short-container-title:

Author:

Bigossi Margherita¹²,Siddiqui Moneeza K¹

Affiliation:

1. Pat McPherson Centre for Pharmacogenetics and Pharmacogenomics, Division of Population Health and Genomics, School of Medicine, Ninewells Hospital and Medical School, University of Dundee , Dundee DD1 9SY , UK

2. Section of Internal Medicine and Thromboembolic Diseases, Department of Medicine, Fondazione Policlinico Universitario A. Gemelli IRCCS , L.go A. Gemelli 8, 00168 Rome , Italy

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

Link

https://academic.oup.com/eurjpc/advance-article-pdf/doi/10.1093/eurjpc/zwac258/47168690/zwac258.pdf

Reference14 articles.

1. Worldwide prevalence of familial hypercholesterolemia: meta-analyses of 11 million subjects;Beheshti;J Am Coll Cardiol,2020

2. Prevalence of familial hypercholesterolemia among the general population and patients with atherosclerotic cardiovascular disease;Hu;Circulation,2020

3. Homozygous autosomal dominant hypercholesterolaemia in The Netherlands: prevalence, genotype–phenotype relationship, and clinical outcome;Sjouke;Eur Heart J,2014

4. The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein;Hobbs;Annu Rev Genet,1990

5. Monogenic hypercholesterolemia: new insights in pathogenesis and treatment;Rader;J Clin Invest,2003

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