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Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson′s disease

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References

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Authors and Affiliations

  1. Center of Neurology, University of Tuebingen, Department of Neurology and Hertie-Institute of Clinical Brain Research, Section for Neurodegenerative Diseases, Hoppe-Seyler Strasse 3, 72076, Tuebingen, Germany

    Alexander Zimprich, Friedrich Asmus, Petra Leitner & Thomas Gasser

  2. Department of Neurology, Klinikum Grosshadern, Ludwig Maximilians University, 80377, Munich, Germany

    Mirna Castro & Benjamin Bereznai

  3. Department of Neurology, University Hospital Graz, Karl Franzens University, 8036, Graz, Austria

    Nikolaus Homann & Erwin Ott

  4. Department of Neurology, Martini Hospital, 9728 NZ, Groningen, The Netherlands

    A. Wijnand F. Rutgers

  5. Paracelsus Elena Klinik, Klinikstrasse 16, 34128, Kassel, Germany

    Gyri Wieditz & Claudia Trenkwalder

Authors
  1. Alexander Zimprich
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  2. Friedrich Asmus
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  3. Petra Leitner
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  4. Mirna Castro
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  5. Benjamin Bereznai
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  6. Nikolaus Homann
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  7. Erwin Ott
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  8. A. Wijnand F. Rutgers
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  9. Gyri Wieditz
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  10. Claudia Trenkwalder
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  11. Thomas Gasser
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Corresponding author

Correspondence to Thomas Gasser.

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Zimprich, A., Asmus, F., Leitner, P. et al. Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson′s disease. Neurogenetics 4, 219–220 (2003). https://doi.org/10.1007/s10048-003-0156-x

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  • DOI: https://doi.org/10.1007/s10048-003-0156-x

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