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• W2763253668 abstract "Annals of NeurologyVolume 82, Issue 4 p. 650-651 Letters/Replies An extremely severe phenotype attributed to WDR81 nonsense mutations Correction(s) for this article Correction: An extremely severe phenotype attributed to WDR81 nonsense mutations Volume 84Issue 5Annals of Neurology pages: 796-796 First Published online: November 21, 2018 Gerarda Cappuccio MD, Gerarda Cappuccio MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorMichele Pinelli MD, PhD, Michele Pinelli MD, PhD orcid.org/0000-0002-5927-1185 Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorAnnalaura Torella PhD, Annalaura Torella PhD Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy Medical Genetics, Department of Biochemistry, Biophysics and General Pathology, University of Campania ‘Luigi Vanvitelli’, Naples, ItalySearch for more papers by this authorGiuseppina Vitiello MD, Giuseppina Vitiello MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, ItalySearch for more papers by this authorAlessandra D'Amico MD, Alessandra D'Amico MD Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, ItalySearch for more papers by this authorMarianna Alagia MD, Marianna Alagia MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorEnnio Del Giudice MD, Ennio Del Giudice MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, ItalySearch for more papers by this authorVincenzo Nigro MD, Vincenzo Nigro MD Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy Medical Genetics, Department of Biochemistry, Biophysics and General Pathology, University of Campania ‘Luigi Vanvitelli’, Naples, ItalySearch for more papers by this authorTUDP, TUDP Telethon Undiagnosed Diseases ProgramSearch for more papers by this authorNicola Brunetti-Pierri MD, Nicola Brunetti-Pierri MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this author Gerarda Cappuccio MD, Gerarda Cappuccio MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorMichele Pinelli MD, PhD, Michele Pinelli MD, PhD orcid.org/0000-0002-5927-1185 Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorAnnalaura Torella PhD, Annalaura Torella PhD Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy Medical Genetics, Department of Biochemistry, Biophysics and General Pathology, University of Campania ‘Luigi Vanvitelli’, Naples, ItalySearch for more papers by this authorGiuseppina Vitiello MD, Giuseppina Vitiello MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, ItalySearch for more papers by this authorAlessandra D'Amico MD, Alessandra D'Amico MD Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, ItalySearch for more papers by this authorMarianna Alagia MD, Marianna Alagia MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this authorEnnio Del Giudice MD, Ennio Del Giudice MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, ItalySearch for more papers by this authorVincenzo Nigro MD, Vincenzo Nigro MD Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, Italy Medical Genetics, Department of Biochemistry, Biophysics and General Pathology, University of Campania ‘Luigi Vanvitelli’, Naples, ItalySearch for more papers by this authorTUDP, TUDP Telethon Undiagnosed Diseases ProgramSearch for more papers by this authorNicola Brunetti-Pierri MD, Nicola Brunetti-Pierri MD Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy Telethon Institute of Genetics and Medicine, Pozzuoli, Naples, ItalySearch for more papers by this author First published: 03 October 2017 https://doi.org/10.1002/ana.25058Citations: 9Read the full textAboutPDF 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume82, Issue4October 2017Pages 650-651 RelatedInformation" @default.
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