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April 07, 2009; 72 (14) Articles

The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

B. Ben Zeev, A. Bebbington, G. Ho, H. Leonard, N. de Klerk, E. Gak, M. Vecksler, J. Christodoulou
First published April 6, 2009, DOI: https://doi.org/10.1212/01.wnl.0000345664.72220.6a
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Article Information

vol. 72 no. 14 1242-1247
DOI: 
https://doi.org/10.1212/01.wnl.0000345664.72220.6a
PubMed: 
19349604
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 April 6, 2009.
Copyright & Usage: 
© 2009

Author Disclosures

    1. B. Ben Zeev, MD,
    2. A. Bebbington, BSc,
    3. G. Ho, MSc,
    4. H. Leonard, MBChB,
    5. N. de Klerk, PhD,
    6. E. Gak, PhD,
    7. M. Vecksler, MSc and
    8. J. Christodoulou, PhD
  1. B. Ben Zeev, MD,
  2. A. Bebbington, BSc,
  3. G. Ho, MSc,
  4. H. Leonard, MBChB,
  5. N. de Klerk, PhD,
  6. E. Gak, PhD,
  7. M. Vecksler, MSc and
  8. J. Christodoulou, PhD
  1. From the Pediatric Neurology Unit, Safra Pediatric Hospital (B.B.Z.), and Sagol Neuroscience Center (E.G.), Sheba Medical Center, Ramat-Gan, Israel; Telethon Institute for Child Health Research (A.B., H.L., N.d.K.), Centre for Child Health Research, University of Western Australia; NSW Centre for Rett Syndrome Research (G.H., J.C.), Children’s Hospital at Westmead, Sydney, Australia; Department of Molecular Genetics and Biochemistry (E.G., M.V.), Sackler Medical School, Tel-Aviv University, Israel; and Disciplines of Paediatrics & Child Health and Genetic Medicine (G.H., J.C.), University of Sydney, Australia.
  1. Address correspondence and reprint requests to Dr. Helen Leonard, Telethon Institute for Child Health Research, Centre for Child Health Research, University of Western Australia, Perth, Australia
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