CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait

• Seval Türkmen ,

  Contributed equally to this work with: Seval Türkmen, Gao Guo

  Affiliation Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany

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• Gao Guo ,

  Contributed equally to this work with: Seval Türkmen, Gao Guo

  Affiliation Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany

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• Masoud Garshasbi,

  Affiliations Max Planck Institute for Molecular Genetics, Berlin, Germany, Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran

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• Katrin Hoffmann,

  Affiliation Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany

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• Amjad J. Alshalah,

  Affiliation University of Babylon, Babylon, Iraq

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• Claudia Mischung,

  Affiliation Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany

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• Andreas Kuss,

  Affiliation Max Planck Institute for Molecular Genetics, Berlin, Germany

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• Nicholas Humphrey,

  Affiliation Centre for Philosophy of Natural and Social Science, London School of Economics, London, United Kingdom

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• Stefan Mundlos,

  Affiliations Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany, Max Planck Institute for Molecular Genetics, Berlin, Germany, Berlin-Brandenburg Center for Regenerative Therapies, Berlin, Germany

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• Peter N. Robinson

  * E-mail: peter.robinson@charite.de

  Affiliations Institute for Medical Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany, Berlin-Brandenburg Center for Regenerative Therapies, Berlin, Germany

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