Associated Papers
Association of C5L2 genetic polymorphisms with coronary artery disease in a Han population in Xinjiang, China.
Zheng YY et al.
Oncotarget, 2017
Genetic polymorphisms in paraoxonase 1 and G protein-coupled receptor 77, and the risk of glucose-6-phosphate dehydrogenase deficiency in a Saudi population.
Alharbi KK
Saudi Medical Journal, 2015
Association of acylation-stimulating protein and receptor gene polymorphisms with coronary heart disease in Han and Hui populations.
Jiang H et al.
International Journal of Clinical and Experimental Medicine, 2015
A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family.
Qu LH et al.
Lipids in Health and Disease, 2014
Circulating C5L2 gene polymorphism is associated with type 2 diabetes mellitus in Saudi population.
Alharbi KK et al.
Molecular Biology Reports, 2013
A novel polymorphism (901G > a) of C5L2 gene is associated with coronary artery disease in Chinese Han and Uyghur population.
Zheng YY et al.
Lipids in Health and Disease, 2013
Relationship between type 2 diabetes mellitus and a novel polymorphism C698T in C5L2 in the Chinese Han population.
Zheng YY et al.
Endocrine, 2012
[Association between apolipoprotein A5 gene polymorphism and coronary heart disease in the Han population from Xinjiang].
Yuan S et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi, 2011
Relationship between a novel polymorphism of the C5L2 gene and coronary artery disease.
Zheng YY et al.
Plos One, 2011
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