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July 15, 2008; 71 (3) Articles

KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes

B. A. Neubauer, S. Waldegger, J. Heinzinger, A. Hahn, G. Kurlemann, B. Fiedler, F. Eberhard, H. Muhle, U. Stephani, S. Garkisch, O. Eeg-Olofsson, U. Müller, T. Sander
First published July 14, 2008, DOI: https://doi.org/10.1212/01.wnl.0000317090.92185.ec
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Article Information

vol. 71 no. 3 177-183
DOI: 
https://doi.org/10.1212/01.wnl.0000317090.92185.ec
PubMed: 
18625963
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 July 14, 2008.
Copyright & Usage: 
© 2008

Author Disclosures

    1. B. A. Neubauer, MD,
    2. S. Waldegger, MD,
    3. J. Heinzinger, MD,
    4. A. Hahn, MD,
    5. G. Kurlemann, MD,
    6. B. Fiedler, MD,
    7. F. Eberhard, MD,
    8. H. Muhle, MD,
    9. U. Stephani, MD,
    10. S. Garkisch,
    11. O. Eeg-Olofsson, MD,
    12. U. Müller, MD and
    13. T. Sander, MD
  1. B. A. Neubauer, MD,
  2. S. Waldegger, MD,
  3. J. Heinzinger, MD,
  4. A. Hahn, MD,
  5. G. Kurlemann, MD,
  6. B. Fiedler, MD,
  7. F. Eberhard, MD,
  8. H. Muhle, MD,
  9. U. Stephani, MD,
  10. S. Garkisch,
  11. O. Eeg-Olofsson, MD,
  12. U. Müller, MD and
  13. T. Sander, MD
  1. From the Departments of Pediatric Neurology (B.A.N., A.H., F.E., S.G.) and Human Genetics (U.M.), University of Giessen-Marburg, Giessen, Germany; Department of Pediatrics (S.W., J.H.), University of Giessen-Marburg, Marburg, Germany; Department of Pediatric Neurology (G.K., B.F.), University of Muenster, Germany; Department of Pediatric Neurology (H.M., U.S.), University of Kiel, Germany; Department of Women’s and Children’s Health (O.E.-O.), Uppsala University, Sweden; and Cologne Center for Genomics (T.S.), University of Cologne, Germany.
  1. Address correspondence and reprint requests to Dr. Bernd A. Neubauer, Department of Pediatric Neurology, University of Giessen-Marburg, Feulgenstrasse 12, D-35385 Giessen, Germany
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