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February 10, 2004; 62 (3) Articles

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease

K. Hedrich, A. Djarmati, N. Schäfer, R. Hering, C. Wellenbrock, P. H. Weiss, R. Hilker, P. Vieregge, L. J. Ozelius, P. Heutink, V. Bonifati, E. Schwinger, A. E. Lang, J. Noth, S. B. Bressman, P. P. Pramstaller, O. Riess, C. Klein
First published February 9, 2004, DOI: https://doi.org/10.1212/01.WNL.0000113022.51739.88
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Article Information

vol. 62 no. 3 389-394
DOI: 
https://doi.org/10.1212/01.WNL.0000113022.51739.88
PubMed: 
14872018
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • Received July 25, 2003
  • Accepted December 4, 2003
  • First Published February 9, 2004.
Copyright & Usage: 
© 2004

Author Disclosures

    1. K. Hedrich, PhD*,
    2. A. Djarmati, BS*,
    3. N. Schäfer, BS,
    4. R. Hering, PhD,
    5. C. Wellenbrock, BS,
    6. P. H. Weiss, MD,
    7. R. Hilker, MD,
    8. P. Vieregge, MD,
    9. L. J. Ozelius, PhD,
    10. P. Heutink, MD,
    11. V. Bonifati, MD,
    12. E. Schwinger, MD,
    13. A. E. Lang, MD,
    14. J. Noth, MD,
    15. S. B. Bressman, MD,
    16. P. P. Pramstaller, MD,
    17. O. Riess, PhD and
    18. C. Klein, MD
  1. K. Hedrich, PhD*,
  2. A. Djarmati, BS*,
  3. N. Schäfer, BS,
  4. R. Hering, PhD,
  5. C. Wellenbrock, BS,
  6. P. H. Weiss, MD,
  7. R. Hilker, MD,
  8. P. Vieregge, MD,
  9. L. J. Ozelius, PhD,
  10. P. Heutink, MD,
  11. V. Bonifati, MD,
  12. E. Schwinger, MD,
  13. A. E. Lang, MD,
  14. J. Noth, MD,
  15. S. B. Bressman, MD,
  16. P. P. Pramstaller, MD,
  17. O. Riess, PhD and
  18. C. Klein, MD
  1. From the Departments of Human Genetics (Drs. Hedrich, Schwinger, and Klein, and A. Djarmati, N. Schäfer, and C. Wellenbrock) and Neurology (Drs. Hedrich, Vieregge, and Klein, and A. Djarmati, N. Schäfer, and C. Wellenbrock), University of Lübeck, Germany; Faculty of Biology (A. Djarmati), University of Belgrade, Serbia; Department of Medical Genetics (Drs. Hering and Riess), University Tübingen, Germany; Department of Neurology (Drs. Weiss and Noth), University of Aachen, Germany; Department of Neurology (Dr. Hilker), University of Cologne, Germany; Department of Molecular Genetics (Dr. Ozelius), Albert Einstein College of Medicine, Bronx, NY; Genetic-Epidemiologic Unit (Drs. Heutink and Bonifati), Department of Clinical Genetics, Department of Epidemiology & Biostatistics, Eramus Medical Center Rotterdam, the Netherlands; Department of Neurological Sciences (Dr. Bonifati), “La Sapienza” University, Rome, Italy; Division of Neurology (Dr. Lang), Department of Medicine, University of Toronto, and Toronto Western Hospital, Canada; Department of Neurology (Dr. Bressman), Beth Israel Medical Center, New York, NY; and Department of Neurology (Dr. Pramstaller), Regional General Hospital, Bolzano, Italy.
  1. Address correspondence and reprint requests to Dr. Christine Klein, Department of Neurology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany; e-mail: klein_ch{at}neuro.mu-luebeck.de
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