PON2 gene variants are associated with clinical manifestations of cardiovascular disease in familial hypercholesterolemia patients
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference40 articles.
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3. Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations;Kotze;Arterioscler. Thromb.,1993
4. Family similarities in the age at coronary death in familial hypercholesterolaemia;Heiberg;Br. Med. J.,1977
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2. Human Paraoxonase-2 (PON2): Protein Functions and Modulation;Antioxidants;2021-02-07
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