PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease

PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease

Abstract Background Severe coronary artery disease (CAD) represents an advanced arterial narrowing, often associated with critical complications like myocardial infarction and angina. This study aimed to comprehensively investigate determinants of severe and multi-vessel CAD manifestations. Methods...

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Bibliographic Details
Main Authors: Cynthia Al Hageh, Siobhán O’Sullivan, Andreas Henschel, Antoine Abchee, Mireille Hantouche, Nantia Iakovidou, Taly Issa, Stephanie Chacar, Moni Nader, Pierre A. Zalloua
Format: Article
Language:English
Published: BMC 2024-10-01
Series:Lipids in Health and Disease
Subjects:
Severe CAD
Multivessel CAD
APOC1
PHACTR1
Online Access:https://doi.org/10.1186/s12944-024-02327-2

Internet

https://doi.org/10.1186/s12944-024-02327-2

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