How Genomics Is Personalizing the Management of Dyslipidemia and Cardiovascular Disease Prevention
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/article/10.1007/s11886-018-1079-3/fulltext.html
Reference59 articles.
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2. Bays HE, Jones PH, Brown WV, Jacobson TA, National Lipid Association. National Lipid Association Annual summary of clinical lipidology 2015. J Clin Lipidol. 2014;8(6 Suppl):S1–36.
3. •• Sturm AC, Knowles JW, Gidding SS, Ahmad ZS, Ahmed CD, Ballantyne CM, et al. Clinical genetic testing for familial hypercholesterolemia: JACC scientific expert panel. J Am Coll Cardiol. 2018;72(6):662–80 New recommendations encouraging genetic testing for all patients with suspected familial hypercholesterolemia.
4. Innerarity TL, Weisgraber KH, Arnold KS, Mahley RW, Krauss RM, Vega GL, et al. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding. Proc Natl Acad Sci U S A. 1987;84(19):6919–23.
5. Myant NB, Gallagher JJ, Knight BL, McCarthy SN, Frostegård J, Nilsson J, et al. Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function. Arterioscler Thromb. 1991;11(3):691–703.
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