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          Institute: MPI für molekulare Genetik     Collection: Research Group Development and Disease     Display Documents



  history
ID: 24441.0, MPI für molekulare Genetik / Research Group Development and Disease
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in caucasian patients with a huntington's disease-like phenotype
Authors:Bauer, Ingrid; Gencik, Martin; Laccone, Franco; Peters, Hartmut; Weber, Bernhard H. F.; Holinski Feder, Elke; Weirich, Helga; Morris-Rosendahl, Deborah J.; Rolfs, Arndt; Gencikova, Alexandra; Bauer, Peter; Wenning, Gregor K.; Epplen, Jörg T.; Holmes, Susan E.; Margolis, Russell L.; Ross, Christopher A.; Riess, Olaf
Language:English
Date of Publication (YYYY-MM-DD):2002-04-23
Title of Journal:Annals of Neurology
Volume:51
Issue / Number:5
Start Page:662
End Page:662
Review Status:not specified
Audience:Experts Only
Abstract / Description:No abstract.
External Publication Status:published
Document Type:Article
Communicated by:Stefan Mundlos
Affiliations:MPI für molekulare Genetik
External Affiliations:Department of Medical Genetics, University of Rostock, Rostock, Germany
Department of Molecular Human Genetics, Ruhr-University, Bochum, Germany
Department of Human Genetics, University of Göttingen, Göttingen, Germany
Department of Medical Genetics, Charité, Humboldt University of Berlin, Berlin, Germany
Institute of Human Genetics, University of Würzburg, Würzburg, Germany
Medizinisch-Genetisches Zentrum, Munich, Germany
Institute of Human Genetics and Anthropology, University of Freiburg, Freiburg, Germany
Department of Neurology, University of Rostock, Rostock, Germany
Department of Medical Genetics, University of Tübingen, Germany
Institute of Medical Genetics, University of Innsbruck, Austria
Department of Neurology, University of Innsbruck, Austria
Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, MD
Program in Cellular and Molecular Medicine, Johns Hopkins University School of Medicine, Baltimore, MD
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