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CORRECTION article

Front. Cardiovasc. Med. , 14 February 2024

Sec. Cardiac Rhythmology

Volume 11 - 2024 | https://doi.org/10.3389/fcvm.2024.1372782

Corrigendum: Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

This article is a correction to:

  1. Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

    1. Read original article
\r\nHans Ebbinghaus Hans Ebbinghaus1*Laura UeberhamLaura Ueberham2Daniela Husser-BollmannDaniela Husser-Bollmann1Andreas BollmannAndreas Bollmann1Ingo PaetschIngo Paetsch1Cosima JahnkeCosima Jahnke1Ulrich LaufsUlrich Laufs2Borislav Dinov\r\nBorislav Dinov3
  • 1Department for Electrophysiology, Heart Center of Leipzig, Leipzig, Germany
  • 2Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, Germany
  • 3Department of Cardiology, Medical University of Giessen, Giessen, Germany

A Corrigendum on

Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease

By Ebbinghaus H, Ueberham L, Husser-Bollmann D, Bollmann A, Laufs U and Dinov B (2023). Front. Cardiovasc. Med. 10:1328802. doi: 10.3389/fcvm.2023.1328802

Error in author list

In the published article, there was an error in the author list, and authors Ingo Paetsch and Cosima Jahnke were erroneously excluded. The corrected author list appears below.

Hans Ebbinghaus1*, Laura Ueberham2, Daniela Husser-Bollmann1, Andreas Bollmann1, Ingo Paetsch1, Cosima Jahnke1, Ulrich Laufs2 and Borislav Dinov3

Affiliations of all authors as they appear in the published original version of the article

1Department for Electrophysiology, Heart Center of Leipzig, Leipzig, Germany, 2Klinik und Poliklinik für Kardiologie, Universitätsklinikum Leipzig, Leipzig, Germany, 3Department of Cardiology, Medical University of Giessen, Giessen, Germany

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: cardiac sarcoidosis, non-ischemic cardiomyopathy, familial cardiomyopathy, ventricular tachyarrhythmias, conduction disease

Citation: Ebbinghaus H, Ueberham L, Husser-Bollmann D, Bollmann A, Paetsch I, Jahnke C, Laufs U and Dinov B (2024) Corrigendum: Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy—a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease. Front. Cardiovasc. Med. 11:1372782. doi: 10.3389/fcvm.2024.1372782

Received: 18 January 2024; Accepted: 25 January 2024;
Published: 14 February 2024.

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

© 2024 Ebbinghaus, Ueberham, Husser- Bollmann, Bollmann, Paetsch, Jahnke, Laufs and Dinov. 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: Hans Ebbinghaus aGFucy5lYmJpbmdoYXVzQG1lZGl6aW4udW5pLWxlaXB6aWcuZGU=

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.

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