An R223P mutation in EXT2 gene causes hereditary multiple exostoses

Human MutationVolume 15, Issue 4 p. 390-391 Mutation and Polymorphism Report An R223P mutation in EXT2 gene causes hereditary multiple exostoses † Yi-Ru Shi, Yi-Ru Shi Department of Medical Research, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorJer-Yuarn Wu, Jer-Yuarn Wu Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Medical Genetics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorFuu-Jen Tsai, Fuu-Jen Tsai Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Pediatrics, China Medical College Hospital, Taichung, Taiwan Department of Medical Genetics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorCheng-Chun Lee, Cheng-Chun Lee Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Neurology, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorChang-Hai Tsai, Chang-Hai Tsai Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Pediatrics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this author Yi-Ru Shi, Yi-Ru Shi Department of Medical Research, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorJer-Yuarn Wu, Jer-Yuarn Wu Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Medical Genetics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorFuu-Jen Tsai, Fuu-Jen Tsai Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Pediatrics, China Medical College Hospital, Taichung, Taiwan Department of Medical Genetics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorCheng-Chun Lee, Cheng-Chun Lee Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Neurology, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this authorChang-Hai Tsai, Chang-Hai Tsai Department of Medical Research, China Medical College Hospital, Taichung, Taiwan Department of Pediatrics, China Medical College Hospital, Taichung, TaiwanSearch for more papers by this author First published: 22 March 2000 https://doi.org/10.1002/(SICI)1098-1004(200004)15:4<390::AID-HUMU35>3.0.CO;2-ECitations: 3 † Communicated by: Mark H. Paalman ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #108 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr108.pdf § Acknowledgments:: The work is funded by a grant (DMR-89-056) from China Medical College Hospital, Taichung, Taiwan. 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 onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume15, Issue4April 2000Pages 390-391 RelatedInformation