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Lancet Psychiatry

Familial chylomicronemia syndrome is a rare genetic disorder estimated to affect 1 to 2 individuals per million and characterized by hypertriglyceridemia, which is caused by mutations in LPL or genes that regulate LPL function which include but are not limited to APOC2, APOA5, GPIHBP1, and lipase maturation factor 1 (LMF1) [19,20]

Explain how membrane lipid and protein components and their structural asymmetries are important for membrane functions in cells

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Randomised controlled trial of L-carnitine as a nutritional supplement in preterm infants