Double-heterozygous autosomal dominant hypercholesterolemia: Clinical characterization of an underreported disease-Reference-Cited by-同舟云学术

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Double-heterozygous autosomal dominant hypercholesterolemia: Clinical characterization of an underreported disease

Published:2016-11 Issue:6 Volume:10 Page:1462-1469
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Sjouke Barbara,Defesche Joep C.,Hartgers Merel L.,Wiegman Albert^ORCID,Roeters van Lennep Jeanine E.,Kastelein John J.,Hovingh G. Kees

Funder

Dr Kastelein is a recipient of the Lifetime Achievement Award of the Dutch Heart Foundation

Dr Hovingh is holder of a Vidi grant

Netherlands Organisation for Scientific Research (NWO). This work is supported by CardioVascular Research Initiative

European Union

Publisher

Elsevier BV

Subject

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

Reference18 articles.

1. Familial Hypercholesterolemia;Goldstein,2001

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

3. Homozygous familial hypercholesterolemia: 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;Cuchel;Eur Heart J,2014

4. Homozygous familial hypercholesterolemia: current perspectives on diagnosis and treatment;Raal;Atherosclerosis,2012

5. Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype-phenotype relationship, and clinical outcome;Sjouke;Eur Heart J,2015

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