British Journal of HaematologyVolume 197, Issue 6 p. 804-804 RETRACTIONFree Access Retraction statement: First report of novel heterozygous WRAP53 p.Ala522Glyfs*8 mutation associated dyskeratosis congenita This article retracts the following: Retracted: First report of novel heterozygous WRAP53 p.Ala522Glyfs*8 mutation associated dyskeratosis congenita Tylan Magnusson, Richard C. Godby, Kimo Bachiashvili, Omer Jamy, Volume 196Issue 4British Journal of Haematology pages: e27-e29 First Published online: October 14, 2021 First published: 25 May 2022 https://doi.org/10.1111/bjh.18282AboutSectionsPDF 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 The above article1 from the British Journal of Haematology, published online on 14 October 2021 in Wiley Online Library (wileyonlinelibrary.com), and in Volume, pp. e27–e29, has been retracted by agreement between the authors, the journal Senior Editor, Prof. Peter Hokland MD, and John Wiley and Sons Ltd. The retraction has been agreed upon following a concern raised to the journal by a third party regarding a possible error in the sequencing of the material used to support the conclusions of the paper. The journal sought independent expertise, which agreed with the third party that the sequencing error invalidates the article's conclusions. The author and the journal have therefore decided to retract the article. The supplementary information for this article was removed at the request of the authors before the article's retraction and with the approval of the journal and publisher. The file included confidential patient information which was not detectable to the naked eye but could be uncovered using software. The journal finds that the errors described are inadvertent and do in not in any way suggest scientific dishonesty on the part of the authors. REFERENCES 1Magnusson T, Godby RC, Bachiashvili K, Jamy O. First report of novel heterozygous WRAP53 p.Ala522Glyfs*8 mutation associated dyskeratosis congenita. Br J Haematol. 2022; 196: e27– 9. https://doi.org/10.1111/bjh.17883Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Volume197, Issue6June 2022Pages 804-804 ReferencesRelatedInformation