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CORRECTION article

Front. Cardiovasc. Med., 15 June 2022
Sec. General Cardiovascular Medicine
Volume 9 - 2022 | https://doi.org/10.3389/fcvm.2022.944834

Corrigendum: Case Report: Family Curse: An SCN5A Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia

This article is a correction to:

  1. Case Report: Family Curse: An SCN5A Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia

    1. Read original article
\nWen Huang,Wen Huang1,2Rui Xu Rui Xu2*Ning GaoNing Gao2Xia WuXia Wu2Cong WenCong Wen3
  • 1Department of Medical Ultrasound, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, China
  • 2Department of Cardiology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Medicine and Health Key Laboratory of Cardiac Electrophysiology and Arrhythmia, Shandong University, Jinan, China
  • 3Department of Cardiology, Shandong Provincial Qianfoshan Hospital, Weifang Medical University, Jinan, China

A Corrigendum on
Case Report: Family Curse: An SCN5A Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia

by Huang, W., Xu, R., Gao, N., Wu, X., and Wen, C. (2022). Front. Cardiovasc. Med. 9:822150. doi: 10.3389/fcvm.2022.822150

In the published article, there was an error regarding the affiliation for Corresponding Author Rui Xu. Instead of “Shandong Medicine and Health Key Laboratory of Cardiac Electrophysiology and Arrhythmia, Department of Cardiology, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Jinan, China,” the affiliation should read “Department of Cardiology, the First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Medicine and Health Key Laboratory of Cardiac Electrophysiology and Arrhythmia, Shandong University, Jinan, China.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: SCN5A, PRKAG2, dilated cardiomyopathy, sudden cardiac death, familial case report

Citation: Huang W, Xu R, Gao N, Wu X and Wen C (2022) Corrigendum: Case Report: Family Curse: An SCN5A Mutation, c.611C>A, p.A204E Associated With a Family History of Dilated Cardiomyopathy and Arrhythmia. Front. Cardiovasc. Med. 9:944834. doi: 10.3389/fcvm.2022.944834

Received: 15 May 2022; Accepted: 30 May 2022;
Published: 15 June 2022.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2022 Huang, Xu, Gao, Wu and Wen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Rui Xu, xuruicn@hotmail.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.