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February 21, 2012; 78 (8) Articles

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy

P. Striano, Y.G. Weber, M.R. Toliat, J. Schubert, C. Leu, R. Chaimana, S. Baulac, R. Guerrero, E. LeGuern, A.-E. Lehesjoki, A. Polvi, A. Robbiano, J.M. Serratosa, R. Guerrini, P. Nürnberg, T. Sander, F. Zara, H. Lerche, C. Marini
First published January 25, 2012, DOI: https://doi.org/10.1212/WNL.0b013e318247ff54
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Article Information

vol. 78 no. 8 557-562
DOI: 
https://doi.org/10.1212/WNL.0b013e318247ff54
PubMed: 
22282645
Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • Received April 14, 2011
  • Accepted August 2, 2011
  • First Published January 25, 2012.

Article Versions

Copyright & Usage: 
Copyright © 2012 by AAN Enterprises, Inc.

Author Disclosures

    1. P. Striano, MD, PhD*,
    2. Y.G. Weber, MD*,
    3. M.R. Toliat, PhD,
    4. J. Schubert,
    5. C. Leu, PhD,
    6. R. Chaimana,
    7. S. Baulac, PhD,
    8. R. Guerrero, PhD,
    9. E. LeGuern, PhD,
    10. A.-E. Lehesjoki, PhD,
    11. A. Polvi, MD,
    12. A. Robbiano, PhD,
    13. J.M. Serratosa, MD, PhD,
    14. R. Guerrini, MD,
    15. P. Nürnberg, PhD,
    16. T. Sander, MD,
    17. F. Zara, PhD,
    18. H. Lerche, MD and
    19. C. Marini, MD, PhD On behalf of the EPICURE Consortium
  1. P. Striano, MD, PhD*,
  2. Y.G. Weber, MD*,
  3. M.R. Toliat, PhD,
  4. J. Schubert,
  5. C. Leu, PhD,
  6. R. Chaimana,
  7. S. Baulac, PhD,
  8. R. Guerrero, PhD,
  9. E. LeGuern, PhD,
  10. A.-E. Lehesjoki, PhD,
  11. A. Polvi, MD,
  12. A. Robbiano, PhD,
  13. J.M. Serratosa, MD, PhD,
  14. R. Guerrini, MD,
  15. P. Nürnberg, PhD,
  16. T. Sander, MD,
  17. F. Zara, PhD,
  18. H. Lerche, MD and
  19. C. Marini, MD, PhD On behalf of the EPICURE Consortium
  1. From the Muscular and Neurodegenerative Diseases Unit, “G. Gaslini” Institute (P.S., A.R., F.Z.), University of Genova, Genova, Italy; Abteilung Neurologie mit Schwerpunkt Epileptologie (Y.G.W., J.S., H.L.), Hertie Institut für klinische Hirnforschung, Universität Tübingen, Tübingen, Germany; Cologne Center for Genomics (M.R.T., C.L., R.C., P.N., T.S.), Universität zu Köln, Köln, Germany. CRICM UPMC-Paris6 UMR-S975/Inserm U975 (S.B., E.L.), Paris, France; Epilepsy Unit, Neurology Service (R.G., J.M.S.), Fundación Jiménez Díaz, Instituto de Investigaciones Sanitarias and CIBERER, Madrid, Spain; Folkhälsan Institute of Genetics, Department of Medical Genetics and Neuroscience Center (A.-E.L., A.P.), University of Helsinki, Helsinki, Finland; IRCCS Stella Maris Foundation (R.G.), University of Pisa, Pisa, Italy; and Child Neurology Unit (R.G., C.M.), Children's Hospital A. Meyer, Florence, Italy.
  1. Correspondence & reprint requests to Prof. Dr. med. Lerche: holger.lerche{at}uni-tuebingen.de
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