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February 07, 2012; 78 (6) Articles

Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers

M. Anheim, A. Elbaz, S. Lesage, A. Durr, C. Condroyer, F. Viallet, P. Pollak, B. Bonaïti, C. Bonaïti-Pellié, A. Brice
First published January 25, 2012, DOI: https://doi.org/10.1212/WNL.0b013e318245f476
M. Anheim
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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
M. Anheim, A. Elbaz, S. Lesage, A. Durr, C. Condroyer, F. Viallet, P. Pollak, B. Bonaïti, C. Bonaïti-Pellié, A. Brice
Neurology Feb 2012, 78 (6) 417-420; DOI: 10.1212/WNL.0b013e318245f476

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Article Information

vol. 78 no. 6 417-420
DOI: 
https://doi.org/10.1212/WNL.0b013e318245f476
PubMed: 
22282650

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 8, 2011
  • Accepted September 29, 2011
  • First Published January 25, 2012.

Article Versions

  • Previous version (January 25, 2012 - 13:02).
  • You are viewing the most recent version of this article.
Copyright & Usage: 
Copyright © 2012 by AAN Enterprises, Inc.

Author Disclosures

    1. M. Anheim, MD, PhD,
    2. A. Elbaz, MD, PhD,
    3. S. Lesage, PhD,
    4. A. Durr, MD, PhD,
    5. C. Condroyer, BS,
    6. F. Viallet, MD, PhD,
    7. P. Pollak, MD,
    8. B. Bonaïti, MSc,
    9. C. Bonaïti-Pellié, MD, PhD and
    10. A. Brice, MD On behalf of the French Parkinson Disease Genetic Group
  1. M. Anheim, MD, PhD,
  2. A. Elbaz, MD, PhD,
  3. S. Lesage, PhD,
  4. A. Durr, MD, PhD,
  5. C. Condroyer, BS,
  6. F. Viallet, MD, PhD,
  7. P. Pollak, MD,
  8. B. Bonaïti, MSc,
  9. C. Bonaïti-Pellié, MD, PhD and
  10. A. Brice, MD On behalf of the French Parkinson Disease Genetic Group
  1. From INSERM, U975 (M.A., S.L., A.D., C.C., A.B.), Paris, France; Pierre and Marie Curie-Paris 6 Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, Pitié-Salpêtrière (M.A., S.L., A.D., C.C., A.B.), Paris, France; Cnrs, UMR 7225, Paris, France (M.A., S.L., A.D., C.C., A.B.); AP-HP, Pitié-Salpêtrière Hospital, Department of Genetics and Cytogenetics (M.A., A.D., A.B.), Paris, France; Centre de Référence des Maladies Neurogénétiques de l'Enfant et de l'Adulte (M.A., A.D., A.B.), Paris, France; INSERM, U708, Neuroepidemiology, F-75013 (A.E.), Paris, France; UPMC University Paris 06, UMR_S708, Neuroepidemiology, F-75005 (A.E.), Paris, France; Department of Neurology (F.V.), Aix-en-Provence, France; Neurology Department (P.P.), Geneva, Switzerland; INRA-GABI, F-78352 (B.B.), Jouy-en-Josas, France; INSERM, U669, F-94807 (B.B., C.B.-P.), Villejuif, France; and University of Paris-Sud, F-94807 (C.B.-P.), Villejuif, France.
  1. Correspondence & reprint requests to Prof. Brice: alexis.brice{at}upmc.fr
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    • Ellen Sidransky, Chief, Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, NIHsidranse@mail.nih.gov
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