Human MutationVolume 13, Issue 5 p. 414-414 Mutation and Polymorphism Report Homozygous mutation 341delG/101X of the glucose-6-phosphatase (G6PC) gene causes glycogen storage disease type Ia (von Gierke disease) in a Chinese patient † Tsang-Ming Ko, Tsang-Ming Ko Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this authorZhi-Cheng Liang, Zhi-Cheng Liang Department of Biology, National Jinan University, Guangzhou, People's Republic of ChinaSearch for more papers by this authorYu-Wan Lin, Yu-Wan Lin Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this authorWuh-Liang Hwu, Wuh-Liang Hwu Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this author Tsang-Ming Ko, Tsang-Ming Ko Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this authorZhi-Cheng Liang, Zhi-Cheng Liang Department of Biology, National Jinan University, Guangzhou, People's Republic of ChinaSearch for more papers by this authorYu-Wan Lin, Yu-Wan Lin Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this authorWuh-Liang Hwu, Wuh-Liang Hwu Department of Medical Genetics, College of Medicine, National Taiwan University, Taipei, TaiwanSearch for more papers by this author First published: 20 May 1999 https://doi.org/10.1002/(SICI)1098-1004(1999)13:5<414::AID-HUMU17>3.0.CO;2-5 † Communicated by: Richard G.H. Cotton ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #48 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr48.pdf § Acknowledgments: This study was supported in part by a grant from the National Science Council of the Republic of China on Taiwan (NSC87-2314-B002-338). The Publisher acknowledges the long interval from receipt to publication of this paper. 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. Volume13, Issue51999Pages 414-414 RelatedInformation