Article

Discovery of <em>SOX5</em> as a New Causative Gene for Atrial Fibrillation

2025-10-14

Abstract excerpt

<h4>Background: </h4> /Objectives: Atrial fibrillation (AF), characteristic of chaotic atrial electrical activity along with ineffective atrial systole, remains the most frequent sustained cardiac dysrhythmia, with an overall lifetime risk for AF being approximately 15% to 40% in the global population. AF is associated with substantially enhanced risks for multiple adverse clinical outcomes, including thromboembol...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: b6f1b8a8-ed0a-592a-aae5-cd3b41c21acd
DOI: 10.20944/preprints202510.1011.v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Discovery of <em>SOX5</em> as a New Causative Gene for Atrial FibrillationDOI 10.20944/preprints202510.1011.v1Read

A SHOX2 loss-of-function mutation underlying familial atrial fibrillationSemantic proximity Read

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.Semantic proximity Read

PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.Semantic proximity Read

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.Semantic proximity Read

Discovery of TBX20 As a Novel Gene Underlying Atrial FibrillationSemantic proximity Read

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.Semantic proximity Read

A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valveSemantic proximity Read

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.Semantic proximity Read

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.Semantic proximity Read

Novel GATA5 loss-of-function mutations underlie familial atrial fibrillationSemantic proximity Read

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.Semantic proximity Read

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.Semantic proximity Read