Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens(University of South Australia), Boukje de Vries(Leiden University), Simona Donatello(Université Libre de Bruxelles), Sarah E. Heron(University of South Australia), Bree Hodgson(University of South Australia), Satyan Chintawar(Université Libre de Bruxelles), Douglas E. Crompton(Northern Health), James N. Hughes(University of Adelaide), Susannah T. Bellows(University of Melbourne), Karl Martin Klein(University of Melbourne), Petra M.C. Callenbach(University Medical Center Groningen), Mark Corbett(South Australia Pathology), Alison Gardner(South Australia Pathology), Sara Kivity(Schneider Children's Medical Center), Xenia Iona(University of South Australia), Brigid M. Regan(University of Melbourne), Claudia M Weller(Leiden University), Denis Crimmins(Central Coast Local Health District), Terence J. O’Brien(The Royal Melbourne Hospital), Rosa Guerrero(Hospital Universitario Fundación Jiménez Díaz), John C. Mulley(University of Adelaide), François Dubeau(McGill University), Laura Licchetta(Institute of Neurological Sciences), Francesca Bisulli(Institute of Neurological Sciences), Patrick Cossette(Centre Hospitalier de l’Université de Montréal), Paul Q. Thomas(University of Adelaide), Jozef Gécz(University of Adelaide), José M. Serratosa(Centre for Biomedical Network Research on Rare Diseases), Oebele F. Brouwer(University Medical Center Groningen), Frédérick Andermann(Montreal Neurological Institute and Hospital), Eva Andermann(Montreal Neurological Institute and Hospital), Arn M. J. M. van den Maagdenberg(Leiden University Medical Center), Massimo Pandolfo(Université Libre de Bruxelles), Samuel F. Berkovic(University of Melbourne), Ingrid E. Scheffer(Royal Children's Hospital)
Nature Genetics
March 31, 2013
Cited by 363Open Access
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