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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Autores principales: A. M. Bea, E. Franco-Marín, V. Marco-Benedí, E. Jarauta, I. Gracia-Rubio, A. Cenarro, F. Civeira, I. Lamiquiz-Moneo
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Medicine
R
Science
Q
Acceso en línea:https://doaj.org/article/771bad6f20e14d9dae2854562ef1bad3
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