Rare exonic deletions of theRBFOX1gene increase risk of idiopathic generalized epilepsy-Reference-Cited by-同舟云学术

Rare exonic deletions of theRBFOX1gene increase risk of idiopathic generalized epilepsy

Published:2013-01-25 Issue:2 Volume:54 Page:265-271
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Lal Dennis,Trucks Holger¹,Møller Rikke S.²,Hjalgrim Helle²,Koeleman Bobby P. C.³,de Kovel Carolien G. F.³,Visscher Frank⁴,Weber Yvonne G.⁵,Lerche Holger⁵,Becker Felicitas⁵,Schankin Christoph J.⁶,Neubauer Bernd A.⁷,Surges Rainer⁸,Kunz Wolfram S.⁸,Zimprich Fritz⁹,Franke Andre¹⁰,Illig Thomas¹¹,Ried Janina S.¹²,Leu Costin¹,Nürnberg Peter¹,Sander Thomas¹, ,

Affiliation:

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

2. Danish Epilepsy Center; Dianalund; Denmark

3. Section Complex Genetics; Department of Medical Genetics; University Medical Center Utrecht; Utrecht; The Netherlands

4. Department of Neurology; Admiraal De Ruyter Hospital; Goes; The Netherlands

5. Department of Neurology and Epileptology; Hertie Institute for Clinical Brain Research; University Hospital Tübingen; Tübingen; Germany

6. Department of Neurology; University of Munich Hospital - Großhadern; Munich; Germany

7. Department of Neuropediatrics; University Medical Clinic Giessen; Giessen; Germany

8. Department of Epileptology; University of Bonn; Bonn; Germany

9. Department of Clinical Neurology; Medical University of Vienna; Vienna; Austria

10. Institute for Clinical Molecular Biology; University Hospital Schleswig-Holstein; Kiel; Germany

11. Hannover Unified Biobank; Hannover Medical School; Hannover; Germany

12. Institute of Genetic Epidemiology; Helmholtz Zentrum München; German Research Center for Environmental Health; Neuherberg; Germany

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12084/fullpdf

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