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- W2743135194 abstract "Aim: Hypertriglyceridemia (HTG) is a common lipid disorder. It is supposed, that really high plasma levels of triglycerides (over 10 mmol/L) have strong genetic background. Rare mutations within the genes for LPL, APOA5, APOC2, GPIHBP1 and LMF1 explain some cases, but in majority of the patients, the disease seems to be polygenic. Accumulation of risky alleles can nonlinearly increase the risk of HTG." @default.
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- W2743135194 date "2017-08-01" @default.
- W2743135194 modified "2023-10-18" @default.
- W2743135194 title "Common polymorphisms as strong predictors of hypertriglyceridemia in Czech population" @default.
- W2743135194 doi "https://doi.org/10.1016/j.atherosclerosis.2017.06.738" @default.
- W2743135194 hasPublicationYear "2017" @default.
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