CORRECTION article

Front. Pediatr., 30 June 2022

Sec. Genetics of Common and Rare Diseases

Volume 10 - 2022 | https://doi.org/10.3389/fped.2022.961964

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family

  • 1. Department of Cardiology, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Fuwai Hospital, Beijing, China

  • 2. Emergency and Critical Care Center, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Fuwai Hospital, Beijing, China

  • 3. Department of Geriatric Cardiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China

In the published article, corresponding author “Xian-Liang Zhou” was assigned the affiliation of “Department of Geriatric Cardiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China.” The affiliation of author “Xian-Liang Zhou” should be “Department of Cardiology, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Fuwai Hospital, Beijing, 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.

Summary

Keywords

Liddle syndrome, pathogenicity, pediatrics, amiloride-sensitive current, longterm prognosis

Citation

Zhang D, Qu Y, Dong X-Q, Lu Y-T, Yang K-Q, Liu X-C, Fan P, Hu Y-X, Yang C-X, Gao L-G, Liu Y-X and Zhou X-L (2022) Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family. Front. Pediatr. 10:961964. doi: 10.3389/fped.2022.961964

Received

05 June 2022

Accepted

06 June 2022

Published

30 June 2022

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

10 - 2022

Updates

Copyright

*Correspondence: Ya-Xin Liu Xian-Liang Zhou

This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics

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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