Exon-disrupting deletions ofNRXN1in idiopathic generalized epilepsy-Reference-Cited by-同舟云学术

Exon-disrupting deletions ofNRXN1in idiopathic generalized epilepsy

Published:2013-01-07 Issue:2 Volume:54 Page:256-264
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Møller Rikke S.¹,Weber Yvonne G.²,Klitten Laura L.,Trucks Holger³,Muhle Hiltrud⁴,Kunz Wolfram S.⁵,Mefford Heather C.⁶,Franke Andre⁷,Kautza Monika⁸,Wolf Peter¹,Dennig Dieter⁹,Schreiber Stefan⁷,Rückert Ina-Maria¹⁰,Wichmann H.-Erich,Ernst Jan P.,Schurmann Claudia¹¹,Grabe Hans J.¹²,Tommerup Niels¹³,Stephani Ulrich⁴,Lerche Holger²,Hjalgrim Helle,Helbig Ingo⁴,Sander Thomas³,

Affiliation:

1. Danish Epilepsy Center; Dianalund; Denmark

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

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

4. Department of Neuropediatrics; University Medical Center Schleswig-Holstein; Christian-Albrechts University; Kiel; Germany

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

6. Division of Genetic Medicine; Department of Pediatrics; University of Washington; Seattle; Washington; U.S.A

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

8. Praxis of Human Genetics; Kiel; Germany

9. Neurological Practice “Am Seelberg”; Stuttgart; Germany

10. Institute of Epidemiology II; Helmholtz Zentrum München - German Research Center for Environmental Health; Neuherberg; Germany

11. Interfaculty Institute for Genetics and Functional Genomics; Ernst-Moritz-Arndt-University Greifswald; Greifswald; Germany

12. Department of Psychiatry and Psychotherapy; Ernst-Moritz-Arndt-University Greifswald; Greifswald; Germany

13. Wilhelm Johannsen Center for Functional Genome Research; University of Copenhagen; Copenhagen; Denmark

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12078/fullpdf

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3. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am J Med Genet B Neuropsychiatr Genet,2010

4. A genetic model for neurodevelopmental disease;Coe;Curr Opin Neurobiol,2012a

5. The genetic variability and commonality of neurodevelopmental disease;Coe;Am J Med Genet C Semin Med Genet,2012b

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