Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia-Reference-Cited by-同舟云学术

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Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia

Published:2016-05-13 Issue:6 Volume:57 Page:994-1003
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Weckhuysen Sarah¹²³⁴⁵,Marsan Elise¹²³⁴,Lambrecq Virginie¹²³⁴⁵,Marchal Cécile⁶,Morin-Brureau Mélanie¹²³⁴,An-Gourfinkel Isabelle¹⁵,Baulac Michel¹²³⁴⁵,Fohlen Martine⁷,Kallay Zetchi Christine⁸,Seeck Margitta⁸,de la Grange Pierre⁹,Dermaut Bart¹⁰¹¹,Meurs Alfred¹²,Thomas Pierre¹³,Chassoux Francine¹⁴,Leguern Eric¹²³⁴¹⁵,Picard Fabienne⁸,Baulac Stéphanie¹²³⁴¹⁵

Affiliation:

1. INSERM; U1127; ICM; Paris France

2. CNRS; UMR 7225; ICM; Paris France

3. Sorbonne Universités; UMR S 1127; UPMC Univ Paris 06; Paris France

4. Institut du Cerveau et de la Moelle épinière; ICM; Paris France

5. Centre de référence épilepsies rares; Epilepsy unit; AP-HP Groupe hospitalier Pitié-Salpêtrière; Paris France

6. CHU de Bordeaux; service d'épileptologie; Bordeaux France

7. Department of Pediatric Neurosurgery; Rothschild Foundation; Paris France

8. Department of Neurology; University Hospitals (HUG) and Medical School of Geneva; Geneva Switzerland

9. Genosplice Institut du Cerveau et de la Moelle épinière; ICM; Paris France

10. Center for Medical Genetics; Ghent University Hospital; Gent Belgium

11. Inserm U1167; Institut Pasteur de Lille; Université de Lille; Lille France

12. Department of Neurology; Ghent University Hospital; Gent Belgium

13. Service de Neurologie; Hôpital Pasteur; Nice France

14. Centre hospitalier Sainte-Anne; Université Paris Descartes; Paris France

15. Département de Génétique et de Cytogénétique; AP-HP Groupe hospitalier Pitié-Salpêtrière; Paris France

Funder

Investissements d'avenir

Fondation Française pour la Recherche sur l'Epilepsie (FFRE)

Fondation pour la Recherche Médicale

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.13391/fullpdf

Reference35 articles.

1. Mutations in DEPDC5 cause familial focal epilepsy with variable foci;Dibbens;Nat Genet,2013

2. Mutations of DEPDC5 cause autosomal dominant focal epilepsies;Ishida;Nat Genet,2013

3. DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy;Picard;Neurology,2014

4. A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population;Martin;Clin Genet,2014

5. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy;Striano;Epilepsia,2015

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4. Epilepsy surgery in children with genetic etiologies: A prospective evaluation of current practices and outcomes;Seizure: European Journal of Epilepsy;2023-12

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