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Rare gene deletions in genetic generalized and Rolandic epilepsies.
Jabbari, Kamel; Bobbili, Dheeraj R; Lal, Dennis; Reinthaler, Eva M; Schubert, Julian; Wolking, Stefan; Sinha, Vishal; Motameny, Susanne; Thiele, Holger; Kawalia, Amit; Altmüller, Janine; Toliat, Mohammad Reza; Kraaij, Robert; van Rooij, Jeroen; Uitterlinden, André G; Ikram, M Arfan; Zara, Federico; Lehesjoki, Anna-Elina; Krause, Roland; Zimprich, Fritz; Sander, Thomas; Neubauer, Bernd A; May, Patrick; Lerche, Holger; Nürnberg, Peter.
Afiliação
  • Jabbari K; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Bobbili DR; Cologne Biocenter, Institute for Genetics, University of Cologne, Cologne, Germany.
  • Lal D; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
  • Reinthaler EM; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Schubert J; Psychiatric and Neurodevelopmental Genetics Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
  • Wolking S; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
  • Sinha V; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
  • Motameny S; Department of Neurology, Medical University of Vienna, Vienna, Austria.
  • Thiele H; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Kawalia A; Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
  • Altmüller J; Institute for Molecular Medicine FIMM, University of Helsinki, Helsinki, Finland.
  • Toliat MR; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Kraaij R; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • van Rooij J; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Uitterlinden AG; Cologne Center for Genomics, University of Cologne, Cologne, Germany.
  • Ikram MA; Institute of Human Genetics, University of Cologne, Cologne, Germany.
  • Zara F; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Lehesjoki AE; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Krause R; Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Zimprich F; Departments of Epidemiology, Neurology, and Radiology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Neubauer BA; Laboratory of Neurogenetics and Neuroscience, Institute G. Gaslini, Genova, Italy.
  • May P; Folkhälsan Institute of Genetics, Folkhälsan Research Center, Helsinki, Finland.
  • Lerche H; Neuroscience Center and Research Programs Unit, Molecular Neurology, University of Helsinki, Helsinki, Finland.
  • Nürnberg P; Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
PLoS One ; 13(8): e0202022, 2018.
Article em En | MEDLINE | ID: mdl-30148849
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção de Genes / Epilepsia Rolândica / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção de Genes / Epilepsia Rolândica / Predisposição Genética para Doença / Estudos de Associação Genética Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha