FEBS LettersVolume 595, Issue 5 p. 667-667 CorrigendumFree Access Corrigendum This article corrects the following: Oct motif variants in Beckwith–Wiedemann syndrome patients disrupt maintenance of the hypomethylated state of the H19/IGF2 imprinting control region Shuichi Kubo, Chihiro Murata, Hanayo Okamura, Taku Sakasegawa, Chiye Sakurai, Kiyotaka Hatsuzawa, Naohiro Hori, Volume 594Issue 10FEBS Letters pages: 1517-1531 First Published online: February 17, 2020 First published: 08 March 2021 https://doi.org/10.1002/1873-3468.14043AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat This article provides corrections to the following parts in the paper by Kubo et al. [[1]]: 1. All C>T is corrected to T>G The position of the assessed single nucleotide variant within the reversed Oct motif (rO) was incorrect. The T>G variant (reference number 23 in the original article), not C>T, was used in this study. The position of the T>G variant is AC123789.6:g.80686T>G, as shown in the corrected Fig. 3A. All mentions of C>T in the text, figures, and tables are corrected to T>G. This error does not affect the overall conclusion. 2. Correction of references On page 1520, ‘The C>T variant occurs in the rO motif [22,23]’ is corrected to ‘The T>G variant occurs in the rO motif [23]’. On page 1527, ‘These three variants were found in patients with BWS who have maternal hIC1 hypermethylation [19–23]’ is corrected to ‘These three variants were found in patients with BWS who have maternal hIC1 hypermethylation [19–21, 23]’. 3. Typographical errors in Fig. 4B In the P-value tables shown on the right side of the plots in Fig. 4B, the labels fr.1 (10 Hp), fr.1 (6 Hp), and fr.1 (3 Hp) are corrected to fr.1 (10 Hp), fr.2 (6 Hp), and fr.3 (3 Hp), respectively. We apologize for the inconvenience that we may have caused by these errors. Reference 1Kubo S, Murata C, Okamura H, Sakasegawa T, Sakurai C, Hatsuzawa K and Hori N (2020) Oct motif variants in Beckwith-Wiedemann syndrome patients disrupt maintenance of the hypomethylated state of the H19/IGF2 imprinting control region. FEBS Lett 594, 1517– 1531. Wiley Online LibraryPubMedWeb of Science®Google Scholar Volume595, Issue5March 2021Pages 667-667 ReferencesRelatedInformation