Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

Human MutationVolume 41, Issue 5 p. 1075-1075 CORRIGENDUMFree Access Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity This article corrects the following: Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity Hanyin Cheng, Simona Capponi, Emma Wakeling, Elaine Marchi, Quan Li, Mengge Zhao, Chunhua Weng, Stefan G. Piatek, Helena Ahlfors, Robert Kleyner, Alan Rope, Aimé Lumaka, Prosper Lukusa, Koenraad Devriendt, Joris Vermeesch, Jennifer E. Posey, Elizabeth E. Palmer, Lucinda Murray, Eyby Leon, Jullianne Diaz, Lisa Worgan, Amali Mallawaarachchi, Julie Vogt, Sonja A. Munnik, Lauren Dreyer, Gareth Baynam, Lisa Ewans, Zornitza Stark, Sebastian Lunke, Ana R. Gonçalves, Gabriela Soares, Jorge Oliveira, Emily Fassi, Marcia Willing, Jeff L. Waugh, Laurence Faivre, Jean-Baptiste Riviere, Sebastien Moutton, Shehla Mohammed, Katelyn Payne, Laurence Walsh, Amber Begtrup, Maria J. Guillen Sacoto, Ganka Douglas, Nora Alexander, Michael F. Buckley, Paul R. Mark, Lesley C. Adès, Sarah A. Sandaradura, James R. Lupski, Tony Roscioli, Pankaj B. Agrawal, Antonie D. Kline, , Kai Wang, H. T. Marc Timmers, Gholson J. Lyon, Volume 41Issue 2Human Mutation pages: 449-464 First Published online: November 25, 2019 First published: 03 March 2020 https://doi.org/10.1002/humu.24003AboutSectionsPDF 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 onEmailFacebookTwitterLinked InRedditWechat Hanyin Cheng, Simona Capponi, Emma Wakeling, Elaine Marchi, Quan Li, Mengge Zhao, Chunhua Weng, Piatek G. Stefan, Helena Ahlfors, Robert Kleyner, Alan Rope, Aimé Lumaka, Prosper Lukusa, Koenraad Devriendt, Joris Vermeesch, Jennifer E. Posey, Elizabeth E. Palmer, Lucinda Murray, Eyby Leon, Jullianne Diaz, Lisa Worgan, Amali Mallawaarachchi, Julie Vogt, Sonja A. de Munnik, Lauren Dreyer, Gareth Baynam, Lisa Ewans, Zornitza Stark, Sebastian Lunke, Ana R. Gonçalves, Gabriela Soares, Jorge Oliveira, Emily Fassi, Marcia Willing, Jeff L. Waugh, Laurence Faivre, Jean-Baptiste Riviere, Sebastien Moutton, Shehla Mohammed, Katelyn Payne, Laurence Walsh, Amber Begtrup, Maria J. Guillen Sacoto, Ganka Douglas, Nora Alexander, Michael F. Buckley, Paul R. Mark, Lesley C. Adès, Sarah A. Sandaradura, James R. Lupski, Tony Roscioli, Pankaj B. Agrawal, Antonie D. Kline, Kai Wang, H. T. Marc Timmers, Gholson J. Lyon. The article to which this Corrigendum refers was published in Human Mutation 41(2): 449-464 (https://onlinelibrary.wiley.com/doi/full/10.1002/HUMU.23936). The corrigendum corrects name of co-author Piatek G. Stefan to Stefan Piatek G. Authors apologize for the error. REFERENCE Cheng, H., Capponi, S., & Wakeling, E., et al. (2020). Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity. Human Mutation, 41, 449– 464. https://doi.org/10.1002/humu.23936Wiley Online LibraryCASWeb of Science®Google Scholar Volume41, Issue5May 2020Pages 1075-1075 ReferencesRelatedInformation