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  • Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia

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Functional genomics
Original article
Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia

Authors

  • Roddy Walsh NIHR Royal Brompton Cardiovascular Biomedical Research Unit, Royal Brompton and Harefield NHS Trust, London, UK PubMed articlesGoogle scholar articles
  • Nicholas S Peters National Heart and Lung Institute, Imperial College, London, UK PubMed articlesGoogle scholar articles
  • Stuart A Cook National Heart and Lung Institute, Imperial College, London, UK Cardiovascular & Metabolic Disorders, Duke National University of Singapore, Singapore, Singapore National Heart Centre Singapore, Singapore, Singapore PubMed articlesGoogle scholar articles
  • James S Ware NIHR Royal Brompton Cardiovascular Biomedical Research Unit, Royal Brompton and Harefield NHS Trust, London, UK National Heart and Lung Institute, Imperial College, London, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Roddy Walsh, Cardiovascular Biomedical Research Unit, Royal Brompton and Harefield NHS Trust, London SW3 6NP, UK; r.walsh{at}rbht.nhs.uk
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Citation

Walsh R, Peters NS, Cook SA, et al
Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia
Journal of Medical Genetics 2014;51:35-44.

Publication history

  • Received July 15, 2013
  • Revised September 6, 2013
  • Accepted September 23, 2013
  • First published October 17, 2013.
Online issue publication 
April 27, 2016

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