A Novel MCPH1 Isoform Complements the Defective Chromosome Condensation of Human MCPH1-Deficient Cells

• Ioannis Gavvovidis ,

  * E-mail: ioannis.gavvovidis@mdc-berlin.de

  Affiliations Department of Human Genetics, University of Würzburg, Würzburg, Germany, Max-Delbrück-Center for Molecular Medicine, Berlin, Germany

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• Isabell Rost,

  Affiliation Department of Human Genetics, University of Würzburg, Würzburg, Germany

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• Marc Trimborn,

  Affiliation Department of Medical Genetics, Charité - Universitaetsmedizin Berlin, Berlin, Germany

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• Frank J. Kaiser,

  Affiliation Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany

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• Josephine Purps,

  Affiliation Department of Human Genetics, Charité - Universitaetsmedizin Berlin, Berlin, Germany

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• Constanze Wiek,

  Affiliation Department of Otorhinolaryngology and Head & Neck Surgery, Heinrich Heine University School of Medicine, Düsseldorf, Germany

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• Helmut Hanenberg,

  Affiliations Department of Otorhinolaryngology and Head & Neck Surgery, Heinrich Heine University School of Medicine, Düsseldorf, Germany, Department of Pediatrics, Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, Indiana, United States of America, Department of Medical & Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, United States of America

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• Heidemarie Neitzel,

  Affiliation Department of Human Genetics, Charité - Universitaetsmedizin Berlin, Berlin, Germany

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• Detlev Schindler

  Affiliation Department of Human Genetics, University of Würzburg, Würzburg, Germany

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