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
© 2022 Zhang, Qu, Dong, Lu, Yang, Liu, Fan, Hu, Yang, Gao, Liu and Zhou.
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: Ya-Xin Liu yaxinliu1978@hotmail.comXian-Liang Zhou zhouxianliang0326@hotmail.com
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.