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Corrigendum
Corrigendum: Correction of Table. Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
Eun-Hee Cho1, Jae Woong Min2, Sun Shim Choi2, Hoon Sung Choi1, Sang-Wook Kim1
Endocrinology and Metabolism 2021;36(2):468.
DOI: https://doi.org/10.3803/EnM.2021.202
Published online: March 24, 2021

1Division of Endocrinology and Metabolism, Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Korea

2Department of Medical Biotechnology, Institute of Bioscience and Biotechnology, Kangwon National University College of Biomedical Science, Chuncheon, Korea

Corresponding author: Sang-Wook Kim. Department of Internal Medicine, Kangwon National University School of Medicine, 156 Baengnyeong-ro, Chuncheon 24289, Korea, Tel: +82-33-258-9169, Fax: +82-33-258-2455, E-mail: sangwookkim@kangwon.ac.kr

Copyright © 2021 Korean Endocrine Society

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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This corrects the article "Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing" on page 296.
Endocrinol Metab 2017;32:296–301.
https://doi.org/10.3803/EnM.2017.32.2.296
In the published article, there was an incorrect amino acid change in Table 1. The “p.Ser383Pro” should be changed to “p.Ser383Leu.” The corrected table is shown below.
We would like to apologize for any inconvenience or misunderstanding.
Table 1
Bioinformatics Analysis of GCK Mutations
Case GCK exon PolyPhen-2/SIFT prediction Amino acid change DUET predicted stability changes (ΔΔG) Reference
Family 1 2 1/Damaging c.92T>C, p.Leu30Pro −2.175 Kcal/mol (Destabilizing) [6]
Family 2 9 1/Damaging c.1151C>T, p.Ser383Leu −0.465 Kcal/mol (Destabilizing) [6]

Two mutations were predicted to be deleterious using online prediction tools. DUET is a web server that uses an integrated computational approach to study missense mutations in proteins; it is available at http://structure.bioc.cam.ac.uk/duet.

GCK, glucokinase; PolyPhen-2, polymorphism phenotyping v2.

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        Corrigendum: Correction of Table. Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
        Endocrinol Metab. 2021;36(2):468  Published online March 24, 2021
        DOI: https://doi.org/10.3803/EnM.2021.202
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      Corrigendum: Correction of Table. Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
      Corrigendum: Correction of Table. Identification of Maturity-Onset Diabetes of the Young Caused by Glucokinase Mutations Detected Using Whole-Exome Sequencing
      Case GCK exon PolyPhen-2/SIFT prediction Amino acid change DUET predicted stability changes (ΔΔG) Reference
      Family 1 2 1/Damaging c.92T>C, p.Leu30Pro −2.175 Kcal/mol (Destabilizing) [6]
      Family 2 9 1/Damaging c.1151C>T, p.Ser383Leu −0.465 Kcal/mol (Destabilizing) [6]
      Table 1 Bioinformatics Analysis of GCK Mutations

      Two mutations were predicted to be deleterious using online prediction tools. DUET is a web server that uses an integrated computational approach to study missense mutations in proteins; it is available at http://structure.bioc.cam.ac.uk/duet.

      GCK, glucokinase; PolyPhen-2, polymorphism phenotyping v2.

      Table 1

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