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Mutations in the Ldlr gene are the most common cause of familial hypercholesterolemia (FH), an autosomal dominant disorder associated with elevated levels of LDL-C and increased risk for premature cardiovascular disease (218)

doi: 10.1016/s0006-291x(03)00979-3

Trends in Food Science & Technology.RekhaS.SinghalA.GuptaP.et al.Low-caloriefat.substitutes2241244 37

It is possible that in D55 heart, LPL derived FA are directed towards oxidative metabolism rather than storage (Figure 2) [94]

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