The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population-Reference-Cited by-同舟云学术

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The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population

Published:2017-12 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Fairoozy R. H.,Futema M.,Vakili R.,Abbaszadegan M. R.,Hosseini S.,Aminzadeh M.,Zaeri H.,Mobini M.,Humphries S. E.,Sahebkar A.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-17181-9.pdf

Reference57 articles.

1. Hobbs, H. H., Brown, M. S. & Goldstein, J. L. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia. Human Mutation 1, 445–466 (1992).

2. Benn, M., Watts, G. F., Tybjaerg-Hansen, A. & Nordestgaard, B. G. Familial Hypercholesterolemia in the Danish General Population: Prevalence, Coronary Artery Disease, and Cholesterol-Lowering Medication. The Journal of Clinical Endocrinology & Metabolism 97, 3956–3964 (2012).

3. Leitersdorf, E., V der Westhuyzen, D., Coetzee, G. & Hobbs, H. Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners. Journal of Clinical Investigation 84, 954 (1989).

4. Moorjani, S. et al. Homozygous familial hypercholesterolemia among French Canadians in Québec province. Arteriosclerosis, Thrombosis, and Vascular Biology 9, 211–216 (1989).

5. Sjouke, B. et al. Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype–phenotype relationship, and clinical outcome. European heart journal 36, 560 (2015).

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