Paraoxonase 1 -L55M polymorphism and coronary heart disease risk in the Chinese population: evidence from a meta-analysis

Author:

ZHANG Kelian1,ZHUO Huilin1,GUO Jingyi2,LI Delong1,DAI Ruozhu1ORCID

Affiliation:

1. Fujian Medical University Affiliated First Quanzhou Hospital, China

2. Jinjiang Municipal Hospital, China

Publisher

FapUNIFESP (SciELO)

Subject

Food Science,Biotechnology

Reference25 articles.

1. Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes;Adkins S.;American Journal of Human Genetics,1993

2. Two-and three-locus haplotypes of the paraoxonase (PON1) gene are associated with coronary artery disease in Asian Indians;Ahmad I.;Gene,2012

3. Mutations in the human paraoxonase 1 gene: frequencies, allelic linkages, and association with coronary artery disease;Cascorbi I.;Pharmacogenetics,1999

4. Study of the association between paraoxonase1 55 Met/Leu, paraoxonase2 148 Ala/Gly and manganese superoxide dismutase (MnSOD) 9 Ala/Val genetic polymorphisms and coronary heart disease;Chi D. S.;Zhonghua Liu Xing Bing Xue Za Zhi,2006

5. The epidemic of the 20(th) century: coronary heart disease;Dalen J. E.;The American Journal of Medicine,2014

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