A de novo SCA14 mutation in an isolated case of late-onset cerebellar ataxia

Authors

  • Judith van Gaalen MD,

    1. Department of Neurology & Donders Institute for Brain, Cognition and Behaviour Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • Sascha Vermeer MD, PhD,

    1. Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
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  • Marjon van Veluw,

    1. Laboratory for DNA Diagnostics, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands
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  • Bart P.C. van de Warrenburg MD, PhD,

    Corresponding author
    1. Department of Neurology & Donders Institute for Brain, Cognition and Behaviour Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    • Correspondence to: Bart P.C. van de Warrenburg, MD, PhD, Department of Neurology & Donders Institute for Brain, Cognition and Behaviour, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands; b.vandewarrenburg@neuro.umcn.nl

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  • Dennis Dooijes PhD

    1. Laboratory for DNA Diagnostics, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, 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.

No abstract is available for this article.

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