Title: A novel mutation, Y103X, and exon skipping in a patient with Hunter disease
Abstract: Human MutationVolume 15, Issue 4 p. 389-389 Mutation and Polymorphism Report A novel mutation, Y103X, and exon skipping in a patient with Hunter disease † Gloria Bonuccelli, Gloria Bonuccelli Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorMirella Filocamo, Mirella Filocamo Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorStefano Regis, Stefano Regis Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorFabio Corsolini, Fabio Corsolini Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorRaffaella Mazzotti, Raffaella Mazzotti Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorRosanna Gatti, Rosanna Gatti Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this author Gloria Bonuccelli, Gloria Bonuccelli Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorMirella Filocamo, Mirella Filocamo Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorStefano Regis, Stefano Regis Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorFabio Corsolini, Fabio Corsolini Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorRaffaella Mazzotti, Raffaella Mazzotti Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this authorRosanna Gatti, Rosanna Gatti Laboratorio di Diagnosi Pre e Postnatale di Malattie Metaboliche, Istituto G.GasliniSearch for more papers by this author First published: 22 March 2000 https://doi.org/10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU30>3.0.CO;2-3Citations: 3 † Communicated by: Mark H. Paalman ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #103 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr103.pdf § Acknowledgments: Cell line and DNA from patients were part of the collection “Cell lines and DNA bank from patient affected by Genetic disease”, supported by Telethon grants (project C.32). AboutPDF 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 onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume15, Issue4April 2000Pages 389-389 RelatedInformation