ANGPTL3 gene variants in subjects with familial combined hyperlipidemia
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DOI: 10.1038/s41598-021-86384-y
Abstract: Angiopoietin-like 3 (ANGPTL3) plays an important role in lipid metabolism in humans. Loss-of-function variants in ANGPTL3 cause a monogenic disease named familial combined hypolipidemia. However, the potential contribution of ANGPTL3 gene in subjects with familial… read more here.
Keywords: subjects familial; angptl3 gene; familial combined; gene ... See more keywords