Your browser doesn't support javascript.
loading
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Behr, Elijah R; Savio-Galimberti, Eleonora; Barc, Julien; Holst, Anders G; Petropoulou, Evmorfia; Prins, Bram P; Jabbari, Javad; Torchio, Margherita; Berthet, Myriam; Mizusawa, Yuka; Yang, Tao; Nannenberg, Eline A; Dagradi, Federica; Weeke, Peter; Bastiaenan, Rachel; Ackerman, Michael J; Haunso, Stig; Leenhardt, Antoine; Kääb, Stefan; Probst, Vincent; Redon, Richard; Sharma, Sanjay; Wilde, Arthur; Tfelt-Hansen, Jacob; Schwartz, Peter; Roden, Dan M; Bezzina, Connie R; Olesen, Morten; Darbar, Dawood; Guicheney, Pascale; Crotti, Lia; Jamshidi, Yalda.
Afiliación
  • Behr ER; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK yjamshid@sgul.ac.uk ebehr@sgul.ac.uk.
  • Savio-Galimberti E; Divisions of Cardiovascular Medicine and Clinical Pharmacology, Vanderbilt University, Nashville, TN, USA.
  • Barc J; Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, Netherlands.
  • Holst AG; Laboratory for Molecular Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark Novo Nordisk A/S, Denmark.
  • Petropoulou E; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK.
  • Prins BP; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK.
  • Jabbari J; Laboratory for Molecular Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark LEO Pharma A/S, Denmark.
  • Torchio M; IRCCS Istituto Auxologico Italiano, Center for Cardiac Arrhythmias of Genetic Origin, Milan, Italy.
  • Berthet M; Inserm, UMR S1166, Faculté de Médecine Pierre et Marie Curie, Paris, France Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France Institute of Cardiometabolism & Nutrition, ICAN, Pitié-Salpêtrière Hospital, Paris, France.
  • Mizusawa Y; Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, Netherlands.
  • Yang T; Divisions of Cardiovascular Medicine and Clinical Pharmacology, Vanderbilt University, Nashville, TN, USA.
  • Nannenberg EA; Department of Clinical Genetics, Academic Medical Center, Amsterdam.
  • Dagradi F; IRCCS Istituto Auxologico Italiano, Center for Cardiac Arrhythmias of Genetic Origin, Milan, Italy.
  • Weeke P; Divisions of Cardiovascular Medicine and Clinical Pharmacology, Vanderbilt University, Nashville, TN, USA.
  • Bastiaenan R; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK.
  • Ackerman MJ; Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA Division of Pediatric Cardiology, Department of Pediatrics & Adolescent Medicine, Mayo Clinic, Rochester, MN, USA.
  • Haunso S; Laboratory for Molecular Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark Department of Medicine and Surgery, University of Copenhagen, Copenhagen, Denmark.
  • Leenhardt A; AP-HP, Hôpital Bichat, Service de Cardiologie et Centre de Référence des Maladies Cardiaques Héréditaires, Paris, France.
  • Kääb S; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, Germany.
  • Probst V; Inserm, UMR 1087, l'institut du Thorax, Nantes, France CHU Nantes, l'institut du Thorax, Service de Cardiologie, Nantes, France.
  • Redon R; Inserm, UMR 1087, l'institut du Thorax, Nantes, France CHU Nantes, l'institut du Thorax, Service de Cardiologie, Nantes, France.
  • Sharma S; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK.
  • Wilde A; Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, Netherlands Princess Al-Jawhara Al-Brahim Centre of Excellence in Research of Hereditary Disorders, Jeddah, Kingdom of Saudi Arabia.
  • Tfelt-Hansen J; Laboratory for Molecular Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark Department of Medicine and Surgery, University of Copenhagen, Copenhagen, Denmark.
  • Schwartz P; IRCCS Istituto Auxologico Italiano, Center for Cardiac Arrhythmias of Genetic Origin, Milan, Italy.
  • Roden DM; Divisions of Cardiovascular Medicine and Clinical Pharmacology, Vanderbilt University, Nashville, TN, USA.
  • Bezzina CR; Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, Netherlands.
  • Olesen M; Laboratory for Molecular Cardiology, The Heart Centre, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark Danish National Research Foundation Centre for Cardiac Arrhythmia, Copenhagen, Denmark.
  • Darbar D; Divisions of Cardiovascular Medicine and Clinical Pharmacology, Vanderbilt University, Nashville, TN, USA.
  • Guicheney P; Inserm, UMR S1166, Faculté de Médecine Pierre et Marie Curie, Paris, France Sorbonne Universités, UPMC Univ Paris 06, UMR S1166, Paris, France Institute of Cardiometabolism & Nutrition, ICAN, Pitié-Salpêtrière Hospital, Paris, France.
  • Crotti L; IRCCS Istituto Auxologico Italiano, Center for Cardiac Arrhythmias of Genetic Origin, Milan, Italy Inserm, UMR 1087, l'institut du Thorax, Nantes, France Department of Molecular Medicine, University of Pavia, Pavia, Italy.
  • Jamshidi Y; Human Genetics Research Centre, ICCS, St George's University of London, London SW17 0RE, UK yjamshid@sgul.ac.uk ebehr@sgul.ac.uk.
Cardiovasc Res ; 106(3): 520-9, 2015 Jun 01.
Article en En | MEDLINE | ID: mdl-25691538
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Síndrome de Brugada / Canal de Sodio Activado por Voltaje NAV1.8 Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Asia / Europa Idioma: En Revista: Cardiovasc Res Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Síndrome de Brugada / Canal de Sodio Activado por Voltaje NAV1.8 Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: America do norte / Asia / Europa Idioma: En Revista: Cardiovasc Res Año: 2015 Tipo del documento: Article