ANGPTL3 gene variants in subjects with familial combined hyperlipidemia

ANGPTL3 gene variants in subjects with familial combined hyperlipidemia

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 combined hyperlipidemia (F...

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Bibliographic Details
Main Authors: A. M. Bea, E. Franco-Marín, V. Marco-Benedí, E. Jarauta, I. Gracia-Rubio, A. Cenarro, F. Civeira, I. Lamiquiz-Moneo
Format: Article
Language:English
Published: Nature Publishing Group 2021-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-86384-y

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