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February 20, 2007; 68 (8) Editorials

Pushing the genetic frontier with facioscapulohumeral muscular dystrophy

Steven A. Greenberg, George W. Padberg
First published February 19, 2007, DOI: https://doi.org/10.1212/01.wnl.0000255905.72867.ec
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Article Information

vol. 68 no. 8 544-545
DOI: 
https://doi.org/10.1212/01.wnl.0000255905.72867.ec
PubMed: 
17310022
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published February 19, 2007.
Copyright & Usage: 
© 2007

Author Disclosures

    1. Steven A. Greenberg, MD and
    2. George W. Padberg, MD, PhD
  1. Steven A. Greenberg, MD and
  2. George W. Padberg, MD, PhD
  1. From the Division of Neuromuscular Disease (S.A.G.), Department of Neurology, Brigham and Women’s Hospital and Children’s Hospital Informatics Program at the Harvard–MIT Division of Health Sciences Technology, Harvard Medical School, Boston, MA; and Department of Neurology (G.W.P.), Radboud University Nijmegen Medical Centre, the Netherlands.
  1. Address correspondence and reprint requests to Dr Greenberg, Department of Neurology, Brigham and Women’s Hospital, 75 Francis St., Boston, MA 02115; e-mail: sagreenberg{at}partners.org.
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