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• W2036691551 abstract "Human MutationVolume 11, Issue S1 p. S34-S37 Mutation in BriefFree Access Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes Leena Karttunen, Leena Karttunen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorTarja Ukkonen, Tarja Ukkonen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorKatariina Kainulainen, Katariina Kainulainen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorAnn-Christine Syvänen, Ann-Christine Syvänen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorLeena Peltonen, Corresponding Author Leena Peltonen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandDept. of Human Molecular Genetics, National Public Health Institute, Mannerheimintie 166, FIN-0030, Helsinki, Finland. Fax: 358-0-4744-480Search for more papers by this author Leena Karttunen, Leena Karttunen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorTarja Ukkonen, Tarja Ukkonen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorKatariina Kainulainen, Katariina Kainulainen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorAnn-Christine Syvänen, Ann-Christine Syvänen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandSearch for more papers by this authorLeena Peltonen, Corresponding Author Leena Peltonen Department of Human Molecular Genetics, National Public Health Institute, FIN-00300 Helsinki, FinlandDept. of Human Molecular Genetics, National Public Health Institute, Mannerheimintie 166, FIN-0030, Helsinki, Finland. Fax: 358-0-4744-480Search for more papers by this author First published: 28 April 2011 https://doi.org/10.1002/humu.1380110112Citations: 11AboutPDF 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 Citing Literature Volume11, IssueS1Supplement: Human Mutation1998Pages S34-S37 ReferencesRelatedInformation" @default.
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• W2036691551 title "Two novel fibrillin-1 mutations resulting in premature termination codons but in different mutant transcript levels and clinical phenotypes" @default.
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