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Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

Authors

  • Cathérine C. S. Delnooz MD,

    1. Radboud University Medical Centre, Department of Neurology Donders Institute for Brian, Cognition and Behaviour, Centre for Neuroscience, Nijmegen, The Netherlands
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  • Ron A. Wevers MD, PhD,

    1. Erasmus Medical Centre, Department of Clinical Genetics, Rotterdam, The Netherlands
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  • Marialuisa Quadri MSc,

    1. UCL Institute of Child Health, Clinical and Molecular Genetics Unit, London, United Kingdom
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  • Peter T. Clayton MD, PhD,

    1. Radboud University Medical Centre, Department of Pathology Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands
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  • Philippa B. Mills PhD,

    1. Radboud University Medical Centre, Department of Pathology Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands
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  • Karin Tuschl MD, PhD,

    1. Radboud University Medical Centre, Department of Pathology Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands
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  • Eric J. Steenbergen MD, PhD,

    1. Radboud University Medical Centre, Department of Neurology Donders Institute for Brian, Cognition and Behaviour, Centre for Neuroscience, Nijmegen, The Netherlands
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  • Vincenzo Bonifati MD, PhD,

    1. UCL Institute of Child Health, Clinical and Molecular Genetics Unit, London, United Kingdom
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  • Bart P. C. van de Warrenburg MD PhD

    Corresponding author
    • Radboud University Medical Centre, Department of Neurology Donders Institute for Brian, Cognition and Behaviour, Centre for Neuroscience, Nijmegen, The Netherlands
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  • Relevant conflicts of interest/financial disclosures: Nothing to report.

  • Full financial disclosures and author roles may be found in the online version of this article.

Correspondence to: Dr. van de Warrenburg; e-mail: B.vandewarrenburg@neuro.umcn.nl

No abstract is available for this article.

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