In the published article, there were errors in affiliations for authors “Iksu Byeo” and “Byungwook Lee.” Instead of “Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South Korea”, it should be “Korea BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea” for both the authors.
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.
Summary
Keywords
Lennox-Gastaut syndrome, epilepsy, whole-exome sequencing, genetic variation, Rare-diseases
Citation
Yang JO, Choi M-H, Yoon J-Y, Lee J-J, Nam SO, Jun SY, Kwon HH, Yun S, Jeon S-J, Byeon I, Halder D, Kong J, Lee B, Lee J, Kang J-W and Kim N-S (2021) Corrigendum: Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families. Front. Genet. 12:669107. doi: 10.3389/fgene.2021.669107
Received
18 February 2021
Accepted
19 February 2021
Published
05 March 2021
Approved by
Frontiers Editorial Office, Frontiers Media SA, Switzerland
Volume
12 - 2021
Updates
Copyright
© 2021 Yang, Choi, Yoon, Lee, Nam, Jun, Kwon, Yun, Jeon, Byeon, Halder, Kong, Lee, Lee, Kang and Kim.
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: Nam-Soon Kim nskim37@kribb.re.krJoon-Won Kang childlove@cnu.ac.kr
This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Genetics
†These authors have contributed equally to this work
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