Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patient.

Human MutationVolume 16, Issue 4 p. 374-374 Mutation and Polymorphism Report Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patient † Gertha Gutierrez, Gertha Gutierrez Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorAndrea Schneider, Andrea Schneider Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorJared Jobs, Jared Jobs Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorHartmut Schmidt, Hartmut Schmidt Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorAndrea Korte, Andrea Korte Institute of Human Genetics, Medical School Hannover, Hannover, GermanySearch for more papers by this authorMichael P. Manns, Michael P. Manns Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorManfred Stuhrmann, Manfred Stuhrmann Institute of Human Genetics, Medical School Hannover, Hannover, GermanySearch for more papers by this author Gertha Gutierrez, Gertha Gutierrez Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorAndrea Schneider, Andrea Schneider Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorJared Jobs, Jared Jobs Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorHartmut Schmidt, Hartmut Schmidt Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorAndrea Korte, Andrea Korte Institute of Human Genetics, Medical School Hannover, Hannover, GermanySearch for more papers by this authorMichael P. Manns, Michael P. Manns Department of Gastroenterology and Hepatology, Medical School Hannover, Hannover, GermanySearch for more papers by this authorManfred Stuhrmann, Manfred Stuhrmann Institute of Human Genetics, Medical School Hannover, Hannover, GermanySearch for more papers by this author First published: 26 September 2000 https://doi.org/10.1002/1098-1004(200010)16:4<374::AID-HUMU16>3.0.CO;2-1Citations: 4 † Communicated by: Mark H. Paalman ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #158 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr158.pdf § Acknowledgments:: We acknowledge the support from the Gesellschaft der Freunde der MHH to MS. This project was supported from the MED-PED (make early diagnosis, prevent early death) project. 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 Volume16, Issue4October 2000Pages 374-374 RelatedInformation