Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation

Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation

Multiple genome-wide association studies (GWAS) have identified numerous loci associated with atrial fibrillation (AF). However, the genes driving these associations and how they contribute to the AF pathogenesis remains poorly understood. To identify genes likely to be driving the observed associat...

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Bibliographic Details
Main Authors: Alexander Guldmann Clausen, Oliver Bundgaard Vad, Julie Husted Andersen, Morten Salling Olesen
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
atrial fibrillation
genetics
arrhythmia
splice site variant
cardiomyopathy
cardiology
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2021.650667/full

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https://www.frontiersin.org/articles/10.3389/fcvm.2021.650667/full

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