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An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK, high risk of VENTRICULAR TACHYCARDIA or VENTRICULAR FIBRILLATION, SYNCOPAL EPISODE, and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.

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Individual Studies
  • Mouse Phenotypes - Conduction disorder of the heart

    Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data

  • OMIM - Conduction disorder of the heart

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data

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Thought leaders and organizations working on research involving brugada syndrome.

  • Charles Antzelevitch
  • Pedro Brugada
  • Arthur A M Wilde
  • Ramon Brugada
  • Josep Brugada
  • Medtronic Bakken Research Center
  • University of Heidelberg
  • Teva Pharmaceutical Industries
  • National Heart, Lung, and Blood Institute (NHLBI)
  • Assistance Publique - Hôpitaux de Paris
  • Masonic Medical Research Laboratory
  • Okayama University Graduate School of Medicine
  • Academic Medical Center
  • University College Hospital
  • Calicut Medical College

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