Analysis ofELP4,SRPX2, and interacting genes in typical and atypical rolandic epilepsy-Reference-Cited by-同舟云学术

Analysis ofELP4,SRPX2, and interacting genes in typical and atypical rolandic epilepsy

Published:2014-07-03 Issue:8 Volume:55 Page:e89-e93
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Reinthaler Eva M.¹,Lal Dennis²³⁴,Jurkowski Wiktor⁵,Feucht Martha⁶,Steinböck Hannelore⁷,Gruber-Sedlmayr Ursula⁸,Ronen Gabriel M.⁹,Geldner Julia¹⁰,Haberlandt Edda¹¹,Neophytou Birgit¹²,Hahn Andreas²,Altmüller Janine⁴¹³,Thiele Holger⁴,Toliat Mohammad R.⁴,Lerche Holger¹⁴,Nürnberg Peter⁴³,Sander Thomas⁴,Neubauer Bernd A.²,Zimprich Fritz¹,

Affiliation:

1. Department of Neurology; Medical University of Vienna; Vienna Austria

2. Department of Neuropediatrics; University Medical Center Giessen and Marburg; Giessen Germany

3. Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD); University of Cologne; Cologne Germany

4. Cologne Center for Genomics; University of Cologne; Cologne Germany

5. Luxembourg Centre for Systems Biomedicine (LCSB); University of Luxembourg; Esch-Belval Luxembourg

6. Department of Pediatrics; Medical University of Vienna; Vienna Austria

7. Private Practice for Pediatrics; Vienna Austria

8. Department of Pediatrics; Medical University of Graz; Graz Austria

9. Department of Pediatrics; McMaster University; Hamilton Ontario Canada

10. Department of Pediatrics; Hospital SMZ Süd; Kaiser-Franz-Josef Spital; Vienna Austria

11. Department of Pediatrics; Medical University of Innsbruck; Innsbruck Austria

12. Department of Neuropediatrics; St. Anna Children's Hospital; Vienna Austria

13. Institute of Human Genetics; University of Cologne; Cologne Germany

14. Department of Neurology and Epileptology; Hertie Institute of Clinical Brain Research; University of Tübingen; Tübingen Germany

Funder

Austrian Science Fund

Deutsche Forschungsgemeinschaft

European Science Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12712/fullpdf

Reference18 articles.

1. Benign childhood focal epilepsies;Guerrini;Epilepsia,2012

2. Atypical rolandic epilepsy;Fejerman;Epilepsia,2009

3. Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes;Vears;Epilepsia,2012

4. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes;Lemke;Nat Genet,2013

5. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction;Lesca;Nat Genet,2013

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