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CORRECTION article

Front. Genet., 05 March 2021
Sec. Genetics of Common and Rare Diseases
Volume 12 - 2021 | https://doi.org/10.3389/fgene.2021.669107
This article is part of the Research Topic New Therapeutic Options for Rare Diseases View all 21 articles

Corrigendum: Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families

This article is a correction to:

  1. Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families

    1. Read original article
\nJin Ok Yang,&#x;Jin Ok Yang1,2†Min-Hyuk Choi,&#x;Min-Hyuk Choi3,4†Ji-Yong YoonJi-Yong Yoon3Jeong-Ju LeeJeong-Ju Lee3Sang Ook NamSang Ook Nam5Soo Young JunSoo Young Jun3Hyeok Hee KwonHyeok Hee Kwon6Sohyun YunSohyun Yun3Su-Jin Jeon,Su-Jin Jeon3,4Iksu ByeonIksu Byeon1Debasish HalderDebasish Halder3Juhyun KongJuhyun Kong5Byungwook LeeByungwook Lee1Jeehun LeeJeehun Lee7Joon-Won Kang Joon-Won Kang8*Nam-Soon Kim, Nam-Soon Kim3,4*
  • 1Korea BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea
  • 2Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, South Korea
  • 3Rare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea
  • 4Department of Functional Genomics, Korea University of Science and Technology, Daejeon, South Korea
  • 5Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, South Korea
  • 6Department of Medical Science and Anatomy, Chungnam National University, Daejeon, South Korea
  • 7Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea
  • 8Department of Pediatrics and Medical Science, Chungnam National University Hospital, College of Medicine, Chungnam National University, Daejeon, South Korea

A Corrigendum on
Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families

by Yang JO, Choi M-H, Yoon J-Y, Lee J-J, Nam SO, Jun SY, et al. (2021). Front. Genet. 11:590924. doi: 10.3389/fgene.2020.590924

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.

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

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.kr; Joon-Won Kang, childlove@cnu.ac.kr

†These authors have contributed equally to this work

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