De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

EuroEPINOMICS RES; Steffen Syrbe; Ulrike B. S. Hedrich; Erik Riesch; Tania Djémié; Stephan A. Müller; Rikke S. Møller; Bridget H. Maher; Laura Hernández-Hernández; Matthis Synofzik; Hande Çağlayan; Mutluay Arslan; José M. Serratosa; Michael Nothnagel; Patrick May; Roland Krause; H. Löffler; Katja Detert; Thomas Dorn; Heinrich Vogt; Günter Krämer; Lüdger Schöls; Primus E. Mullis; Tarja Linnankivi; Anna-Elina Lehesjoki; Katalin Štěrbová; Dana Craiu; Dorota Hoffman‐Zacharska; Christian Korff; Yvonne Weber; Maja Steinlin; Sabina Gallati; Astrid Bertsche; Matthias K. Bernhard; Andreas Merkenschlager; Wieland Kieß; Michael Gonzalez; Stephan Züchner; Aarno Palotie; Arvid Suls; Peter De Jonghe; Ingo Helbig; Saskia Biskup; Markus Wolff; Snezana Maljevic; Rebecca Schüle; Sanjay M. Sisodiya; Sarah Weckhuysen; Holger Lerche; Johannes R. Lemke

doi:10.1038/ng.3239

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

EuroEPINOMICS RES, Steffen Syrbe(Hertie Institute for Clinical Brain Research), Ulrike B. S. Hedrich(CeGaT (Germany)), Erik Riesch(University of Antwerp), Tania Djémié(University of Antwerp), Stephan A. Müller(Hertie Institute for Clinical Brain Research), Rikke S. Møller(University of Southern Denmark), Bridget H. Maher(National Hospital for Neurology and Neurosurgery), Laura Hernández-Hernández(German Center for Neurodegenerative Diseases), Matthis Synofzik(German Center for Neurodegenerative Diseases), Hande Çağlayan(Turkish Armed Forces), Mutluay Arslan(Turkish Armed Forces), José M. Serratosa(University of Cologne), Michael Nothnagel(University of Cologne), Patrick May(University of Luxembourg), Roland Krause(University of Luxembourg), H. Löffler(Hertie Institute for Clinical Brain Research), Katja Detert(Hertie Institute for Clinical Brain Research), Thomas Dorn(Swiss Epilepsy Center), Heinrich Vogt(Swiss Epilepsy Center), Günter Krämer(German Center for Neurodegenerative Diseases), Lüdger Schöls(University Hospital of Bern), Primus E. Mullis(University of Helsinki), Tarja Linnankivi(University of Helsinki), Anna-Elina Lehesjoki(University of Helsinki), Katalin Štěrbová(Carol Davila University of Medicine and Pharmacy), Dana Craiu(Carol Davila University of Medicine and Pharmacy), Dorota Hoffman‐Zacharska(University Hospital of Geneva), Christian Korff(University Hospital of Geneva), Yvonne Weber(University Hospital of Bern), Maja Steinlin(University Hospital of Bern), Sabina Gallati(University Hospital of Bern), Astrid Bertsche, Matthias K. Bernhard, Andreas Merkenschlager, Wieland Kieß(University of Miami), Michael Gonzalez(University of Miami), Stephan Züchner(University of Helsinki), Aarno Palotie(University of Helsinki), Arvid Suls(University of Antwerp), Peter De Jonghe(Children's Hospital of Philadelphia), Ingo Helbig(Children's Hospital of Philadelphia), Saskia Biskup(CeGaT (Germany)), Markus Wolff(Hertie Institute for Clinical Brain Research), Snezana Maljevic(University of Miami), Rebecca Schüle(University Hospital of Bern), Sanjay M. Sisodiya(University of Antwerp), Sarah Weckhuysen(University of Antwerp), Holger Lerche(Hertie Institute for Clinical Brain Research), Johannes R. Lemke(University Hospital of Bern)

Nature Genetics

March 9, 2015

10.1038/ng.3239

Cited by 273Open Access

Full Text

Abstract

Related Papers

No related papers found

Powered by citation graph analysis