Phenylketonuria mutations in southern Chinese detected by denaturing gradient gel electrophoresis in exon 7 of PAH gene

Journal of Inherited Metabolic DiseaseVolume 18, Issue 6 p. 753-754 Short Reports Phenylketonuria mutations in southern Chinese detected by denaturing gradient gel electrophoresis in exon 7 of PAH gene X. F. Gu, X. F. Gu Shanghai Institute for Pediatric Research, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this authorM. Zhang, M. Zhang Xin Hua Hospital, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this authorR. G. Chen, R. G. Chen Shanghai Institute for Pediatric Research, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this author X. F. Gu, X. F. Gu Shanghai Institute for Pediatric Research, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this authorM. Zhang, M. Zhang Xin Hua Hospital, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this authorR. G. Chen, R. G. Chen Shanghai Institute for Pediatric Research, Shanghai Second Medical University, Shanghai, People's Republic of ChinaSearch for more papers by this author First published: 01 November 1995 https://doi.org/10.1007/BF02436769Citations: 4 Shanghai Institute of Pediatric Research, 1665 Kong Jing Road, Shanghai, 200092, People's Republic of China 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. References 1Chen RG, Pan XS, Qian DL et al (1989) Twenty-one cases of phenylketonuria out of 348 767 newborns in Shanghai, China. J Inher Metab Dis, 12: 485–485, . 2Eisensmith RC, Woo SLC (1992) Molecular base of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene. Hum Mutat, 1: 13–23, . 3Lerman LS, Silverstein K (1987) Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. Methods Enzymol, 155: 482–501. 4Myers RM, Maniatis T, Lerman LS (1987) Detection and localisation of single base changes by denaturing gradient gel electrophoresis. Methods Enzymol, 155: 501–527, . 5Wang M, Fang PL, Yuang LF et al (1992) Detection of mutation in phenylalanine hydroxylase gene and prenatal diagnosis. Zhong Hua Yi Xue Za Zhi (J Chinese Med), 72: 670–673. Citing Literature Volume18, Issue6November 1995Pages 753-754 ReferencesRelatedInformation