Mutations inTNK2in severe autosomal recessive infantile onset epilepsy-Reference-Cited by-同舟云学术

Mutations inTNK2in severe autosomal recessive infantile onset epilepsy

Published:2013-09 Issue:3 Volume:74 Page:496-501
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Hitomi Yuki¹,Heinzen Erin L.¹,Donatello Simona²,Dahl Hans-Henrik³,Damiano John A.³,McMahon Jacinta M.³,Berkovic Samuel F.³,Scheffer Ingrid E.³⁴⁵,Legros Benjamin⁶,Rai Myriam²,Weckhuysen Sarah⁷⁸,Suls Arvid⁷⁸,De Jonghe Peter⁷⁸,Pandolfo Massimo²⁶,Goldstein David B.¹,Van Bogaert Patrick⁹,Depondt Chantal²⁶

Affiliation:

1. Duke Center for Human Genome Variation; Duke University School of Medicine; Durham NC

2. Laboratory of Experimental Neurology; Université Libre de Bruxelles; Brussels Belgium

3. Epilepsy Research Centre, Department of Medicine; University of Melbourne; Austin Health Melbourne Australia

4. Florey Institute; Melbourne Australia

5. Department of Paediatrics, Royal Children's Hospital; University of Melbourne; Melbourne Australia

6. Department of Neurology, Erasme Hospital; Université Libre de Bruxelles; Brussels Belgium

7. Neurogenetics Group; Department of Molecular Genetics; VIB Antwerp Belgium

8. Laboratory of Neurogenetics, Institute Born-Bunge; University of Antwerp; Antwerp Belgium

9. Department of Neuropediatrics, Erasme Hospital; Free University of Brussels; Brussels Belgium

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.23934/fullpdf

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