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Erratum| Volume 62, 100146, 2021

Erratum: Genetic testing for familial hypercholesterolemia—past, present, and future

Open AccessPublished:November 15, 2021DOI:https://doi.org/10.1016/j.jlr.2021.100146
Erratum: Genetic testing for familial hypercholesterolemia—past, present, and future
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      • Genetic testing for familial hypercholesterolemia—past, present, and future
        Journal of Lipid ResearchVol. 62
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          In the early 1980s, the Nobel Prize winning cellular and molecular work of Mike Brown and Joe Goldstein led to the identification of the LDL receptor gene as the first gene where mutations cause the familial hypercholesterolemia (FH) phenotype. We now know that autosomal dominant monogenic FH can be caused by pathogenic variants of three additional genes (APOB/PCSK9/APOE) and that the plasma LDL-C concentration and risk of premature coronary heart disease differs according to the specific locus and associated molecular cause.
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      Volumn 62, Article 100139
      An error was noticed in the caption to Fig. 2. The first sentence of the caption included the reference citation “data from Huijgen et al. (46).” However, reference 46 is an article by Humphries et al. Therefore, the correct reference citation in the first sentence of the Fig. 2 caption is “data from Humphries et al. (46).”

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      Published online: November 15, 2021

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      DOI: https://doi.org/10.1016/j.jlr.2021.100146

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      © 2021 The Authors. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology.

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      ISSN 0022-2275
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