A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease Communicated by Mark H. Paalman Online Citation: Human Mutation, Mutation and Polymorphism Report #212 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr212.pdf Acknowledgments: This work was supported by the Polish State Committee for Scientific Research (grants 4p05E00815 and 2266/ IA/167/97) and the Fund for Scientific Research (FWO - Flanders, Belgium).

Abstract

Human MutationVolume 17, Issue 2 p. 157-157 Mutation and Polymorphism Report A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease † Andrzej Kochanski, Andrzej Kochanski Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorAnn Lofgren, Ann Lofgren Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorHanna Jedrzejowska, Hanna Jedrzejowska Neuromuscular Medical Research Unit Polish Academy of Sciences, Warsaw, PolandSearch for more papers by this authorBarbara Ryniewicz, Barbara Ryniewicz Neurology Department Medical University, Warsaw, PolandSearch for more papers by this authorMalwina Czarny-Ratajczak, Malwina Czarny-Ratajczak Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorAnna-Maria Barciszewska, Anna-Maria Barciszewska Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorJoanna Samocko, Joanna Samocko Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorIrena Hausmanowa-Petrusewicz, Irena Hausmanowa-Petrusewicz Neuromuscular Medical Research Unit Polish Academy of Sciences, Warsaw, PolandSearch for more papers by this authorPeter De Jonghe, Peter De Jonghe Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorVincent Timmerman, Vincent Timmerman Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorAnna Latos-Bielenska, Anna Latos-Bielenska Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this author Andrzej Kochanski, Andrzej Kochanski Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorAnn Lofgren, Ann Lofgren Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorHanna Jedrzejowska, Hanna Jedrzejowska Neuromuscular Medical Research Unit Polish Academy of Sciences, Warsaw, PolandSearch for more papers by this authorBarbara Ryniewicz, Barbara Ryniewicz Neurology Department Medical University, Warsaw, PolandSearch for more papers by this authorMalwina Czarny-Ratajczak, Malwina Czarny-Ratajczak Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorAnna-Maria Barciszewska, Anna-Maria Barciszewska Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorJoanna Samocko, Joanna Samocko Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this authorIrena Hausmanowa-Petrusewicz, Irena Hausmanowa-Petrusewicz Neuromuscular Medical Research Unit Polish Academy of Sciences, Warsaw, PolandSearch for more papers by this authorPeter De Jonghe, Peter De Jonghe Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorVincent Timmerman, Vincent Timmerman Flanders Interuniversity Institute for Biotechnology (VIB), Born-Bunge Foundation (BBS), Department of Biochemistry, University of Antwerp (UIA), Antwerpen, BelgiumSearch for more papers by this authorAnna Latos-Bielenska, Anna Latos-Bielenska Chair and Department of Medical Genetics, Karol Marcinkowski University of Medical Sciences, Poznan, PolandSearch for more papers by this author First published: 23 January 2001 https://doi.org/10.1002/1098-1004(200102)17:2<157::AID-HUMU22>3.0.CO;2-E † Communicated by Mark H. Paalman ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #212 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr212.pdf § Acknowledgments: This work was supported by the Polish State Committee for Scientific Research (grants 4p05E00815 and 2266/ IA/167/97) and the Fund for Scientific Research (FWO - Flanders, Belgium). 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume17, Issue2February 2001Pages 157-157 RelatedInformation