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August 13, 2002; 59 (3) Articles

X-linked myoclonic epilepsy with spasticity and intellectual disability

Mutation in the homeobox gene ARX

I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, J. C. Mulley
First published August 13, 2002, DOI: https://doi.org/10.1212/WNL.59.3.348
I. E. Scheffer
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R. H. Wallace
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F. L. Phillips
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P. Hewson
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K. Reardon
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G. Parasivam
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P. Stromme
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S. F. Berkovic
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Citation
X-linked myoclonic epilepsy with spasticity and intellectual disability
Mutation in the homeobox gene ARX
I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, J. C. Mulley
Neurology Aug 2002, 59 (3) 348-356; DOI: 10.1212/WNL.59.3.348

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Article Information

vol. 59 no. 3 348-356
DOI: 
https://doi.org/10.1212/WNL.59.3.348
PubMed: 
12177367

Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • Received December 4, 2001
  • Accepted April 15, 2002
  • First Published August 13, 2002.

Copyright & Usage: 
© 2002

Author Disclosures

    1. I. E. Scheffer, MBBS, PhD,
    2. R. H. Wallace, PhD,
    3. F. L. Phillips, BSc,
    4. P. Hewson, MD, BS,
    5. K. Reardon, MBBS,
    6. G. Parasivam, MSc,
    7. P. Stromme, MD, PhD,
    8. S. F. Berkovic, MD, BS,
    9. J. Gecz, PhD and
    10. J. C. Mulley, PhD
  1. I. E. Scheffer, MBBS, PhD,
  2. R. H. Wallace, PhD,
  3. F. L. Phillips, BSc,
  4. P. Hewson, MD, BS,
  5. K. Reardon, MBBS,
  6. G. Parasivam, MSc,
  7. P. Stromme, MD, PhD,
  8. S. F. Berkovic, MD, BS,
  9. J. Gecz, PhD and
  10. J. C. Mulley, PhD
  1. From the Department of Medicine (Neurology) (Drs. Scheffer and Berkovic, F.L. Phillips, and G. Parasivam), University of Melbourne, Epilepsy Research Institute, Austin & Repatriation Medical Centre; Department of Neurology (Drs. Scheffer and Berkovic), Royal Children’s Hospital; Neurosciences (Dr. Scheffer), Monash Medical Centre, Melbourne; Cytogenetics and Molecular Genetics (Drs. Wallace, Stromme, Gecz, and Mulley), Women’s and Children’s Hospital, Adelaide, South Australia; Paediatrics (Dr. Hewson), Barwon Health The Geelong Hospital, Geelong, Victoria; Neurology (K. Reardon), St. Vincent’s Hospital, Melbourne, Victoria; and Paediatrics (Dr. Gecz), The University of Adelaide, Australia.
  1. Address correspondence and reprint requests to Associate Professor Ingrid Scheffer, Epilepsy Research Institute, Austin & Repatriation Medical Centre, Level 1, Neurosciences Building, Repatriation Campus, Banksia Street, West Heidelberg VIC 3081, Australia; e-mail: scheffer{at}unimelb.edu.au
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