ANGPTL3 gene variants in subjects with familial combined hyperlipidemia

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 (FCHL) has...

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Publicat a:Sci Rep
Autors principals: Bea, A. M., Franco-Marín, E., Marco-Benedí, V., Jarauta, E., Gracia-Rubio, I., Cenarro, A., Civeira, F., Lamiquiz-Moneo, I.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2021
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7997994/
https://ncbi.nlm.nih.gov/pubmed/33772079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-86384-y
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