In the original article, there was an error. Incorrect information was published in the abstract.
A correction has been made to Abstract, second sentence:
“We systematically assessed the relationship between stroke and three 9p21 loci (rs2383206, rs2383207, and rs10757278) in this meta-analysis.”
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.
Statements
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
ischemic stroke, chromosome 9p21, rs2383206, rs2383207, rs10757278, Chinese
Citation
Hu X, Wang D, Cui C and Wu Q (2022) Corrigendum: Association of single-nucleotide polymorphisms of rs2383206, rs2383207, and rs10757278 with stroke risk in the Chinese population: A meta-analysis. Front. Genet. 13:980218. doi: 10.3389/fgene.2022.980218
Received
28 June 2022
Accepted
09 September 2022
Published
10 October 2022
Volume
13 - 2022
Edited and reviewed by
Sarah H. Elsea, Baylor College of Medicine, United States
Updates
Copyright
© 2022 Hu, Wang, Cui and Wu.
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: Qingjian Wu, wqw110@163.com
†These authors have contributed equally to this work and share first authorship
This article was submitted to Neurogenomics, a section of the journal Frontiers in Genetics
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.