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Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse.
Hadji-Turdeghal, Katra; Andreasen, Laura; Hagen, Christian M; Ahlberg, Gustav; Ghouse, Jonas; Bækvad-Hansen, Marie; Bybjerg-Grauholm, Jonas; Hougaard, David M; Hedley, Paula; Haunsø, Stig; Svendsen, Jesper H; Kanters, Jørgen K; Jepps, Thomas A; Skov, Morten W; Christiansen, Michael; Olesen, Morten S.
Afiliação
  • Hadji-Turdeghal K; Laboratory for Molecular Cardiology, Department of Cardiology, The Heart Centre, Rigshospitalet (Copenhagen University Hospital), Copenhagen, Denmark.
  • Andreasen L; Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark.
  • Hagen CM; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Ahlberg G; Laboratory for Molecular Cardiology, Department of Cardiology, The Heart Centre, Rigshospitalet (Copenhagen University Hospital), Copenhagen, Denmark.
  • Ghouse J; Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark.
  • Bækvad-Hansen M; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Bybjerg-Grauholm J; Department of Congenital Disorders, Statens Serum Institute, Copenhagen, Denmark.
  • Hougaard DM; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Copenhagen, Denmark.
  • Hedley P; Laboratory for Molecular Cardiology, Department of Cardiology, The Heart Centre, Rigshospitalet (Copenhagen University Hospital), Copenhagen, Denmark.
  • Haunsø S; Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark.
  • Svendsen JH; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Kanters JK; Laboratory for Molecular Cardiology, Department of Cardiology, The Heart Centre, Rigshospitalet (Copenhagen University Hospital), Copenhagen, Denmark.
  • Jepps TA; Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark.
  • Skov MW; Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Christiansen M; Department of Congenital Disorders, Statens Serum Institute, Copenhagen, Denmark.
  • Olesen MS; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Copenhagen, Denmark.
Cardiovasc Res ; 116(1): 138-148, 2020 01 01.
Article em En | MEDLINE | ID: mdl-31049583
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síncope / Cromossomos Humanos Par 2 / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Fatores de Transcrição Kruppel-Like Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged / Newborn País/Região como assunto: Europa Idioma: En Revista: Cardiovasc Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Dinamarca País de publicação: Reino Unido
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síncope / Cromossomos Humanos Par 2 / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Fatores de Transcrição Kruppel-Like Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged / Newborn País/Região como assunto: Europa Idioma: En Revista: Cardiovasc Res Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Dinamarca País de publicação: Reino Unido