Title : A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug.

Pub. Date : 2019 Jan 3

PMID : 30606120






1 Functional Relationships(s)
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1 METHODS: We here report that a recently identified genetic variant, c.553G > T in the APOA5 gene which causes a substitution of a cysteine for a glycine residue at amino acid residue 185(G185C) is also associated with increased TG levels. Glycine apolipoprotein A5 Homo sapiens