A common missense mutation (C210G) in the LDL receptor gene among Norwegian familial hypercholesterolemia subjects

Abstract

Human MutationVolume 7, Issue 1 p. 70-71 Mutations in Brief A common missense mutation (C210G) in the LDL receptor gene among Norwegian familial hypercholesterolemia subjects Hilde Sundvold, Hilde Sundvold Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorKari Solberg, Kari Solberg Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorSerena Tonstad, Serena Tonstad Lipid Clinic, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this authorOlaug K. Rødningen, Olaug K. Rødningen Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorLeiv Ose, Leiv Ose Research Forum, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorKåre Berg, Kåre Berg Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, Norway Institute of Medical Genetics, University of Oslo, Oslo, NorwaySearch for more papers by this authorTrond P. Leren, Corresponding Author Trond P. Leren Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwayDepartment of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, Norway; Fax: 47-2-211-9868Search for more papers by this author Hilde Sundvold, Hilde Sundvold Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorKari Solberg, Kari Solberg Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorSerena Tonstad, Serena Tonstad Lipid Clinic, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this authorOlaug K. Rødningen, Olaug K. Rødningen Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorLeiv Ose, Leiv Ose Research Forum, Ullevál University Hospital, University of Oslo, Oslo, NorwaySearch for more papers by this authorKåre Berg, Kåre Berg Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, Norway Institute of Medical Genetics, University of Oslo, Oslo, NorwaySearch for more papers by this authorTrond P. Leren, Corresponding Author Trond P. Leren Department of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, NorwayDepartment of Medical Genetics, Ullevál University Hospital, University of Oslo, Oslo, Norway; Fax: 47-2-211-9868Search for more papers by this author First published: 1996 https://doi.org/10.1002/(SICI)1098-1004(1996)7:1<70::AID-HUMU12>3.0.CO;2-PCitations: 7AboutPDF 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume7, Issue11996Pages 70-71 RelatedInformation