Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher–Like Disease in Humans

• Oliver Tress,

  Affiliation Institute of Genetics, Division of Molecular Genetics, University of Bonn, Bonn, Germany

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• Marta Maglione,

  Affiliation Cellular Neurosciences, Max-Delbrück Center for Molecular Medicine, Berlin, Germany

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• Armin Zlomuzica,

  Affiliation Center for the Study and Treatment of Mental Health, Ruhr-Universität Bochum, Bochum, Germany

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• Dennis May,

  Affiliation Institute of Genetics, Division of Molecular Genetics, University of Bonn, Bonn, Germany

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• Nikolai Dicke,

  Affiliation Institute of Genetics, Division of Molecular Genetics, University of Bonn, Bonn, Germany

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• Joachim Degen,

  Affiliation Institute of Genetics, Division of Molecular Genetics, University of Bonn, Bonn, Germany

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• Ekrem Dere,

  Affiliation Université Pierre et Marie Curie (Paris VI), UMR 7102, Neurobiologie des Processus Adaptatifs, Paris, France

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• Helmut Kettenmann,

  Affiliation Cellular Neurosciences, Max-Delbrück Center for Molecular Medicine, Berlin, Germany

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• Dieter Hartmann,

  Affiliation Department of Anatomy, Division of Neuroanatomy, University of Bonn, Bonn, Germany

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• Klaus Willecke

  * E-mail: k.willecke@uni-bonn.de

  Affiliation Institute of Genetics, Division of Molecular Genetics, University of Bonn, Bonn, Germany

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