Genetic Testing for Familial Hypercholesterolemia in Clinical Practice
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11883-023-01094-2.pdf
Reference114 articles.
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2. Austin MA, Hutter CM, Zimmern RL, Humphries SE. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review. Am J Epidemiol. 2004;160:407–20.
3. Williams KB, Horst M, Young M, et al. Clinical characterization of familial hypercholesterolemia due to an Amish founder mutation in apolipoprotein B. BMC Cardiovasc Disord. 2022;22:109.
4. Akioyamen LE, Genest J, Shan SD, Reel RL, Albaum JM, Chu A, et al. Estimating the prevalence of heterozygous familial hypercholesterolaemia: a systematic review and meta-analysis. BMJ Open. 2017;7:e016461.
5. Abul-Husn NS, Manickam K, Jones LK, et al. Genetic identification of familial hypercholesterolemia within a single US health care system. Science. 2016. https://doi.org/10.1126/science.aaf7000.
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1. Genetic testing for familial hypercholesterolemia;Current Opinion in Lipidology;2024-02-01
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