Author Information

Brugada syndrome caused by a 3p22.2 deletion including SCN5A and SCN10A defined using medium coverage whole exome sequencing

Rosalyn Jewell1*, Susan Clasper2, Stephen P. Page3, Christopher M. Watson4,5, Oonagh Claber6, Christopher Hayes7, Kate Sergeant2, Andrea Coates5, Laura A. Crinnion4,5, Sarah Hewitt5, Matthieu J. Miossec8,9, Mauro Santibanez-Koref8, Kathryn Ashcroft1, David T. Bonthron1,4, Bernard Keavney10, Paul Brennan6, Jennifer Thomson1

  1. Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, LS7 4SA, UK
  2. Genetics Laboratories, Oxford University Hospitals NHS Trust, Oxford, OX3 7LE, UK
  3. Department of Cardiology, Leeds Teaching Hospitals NHS Trust, Leeds, LS1 3EX, UK
  4. School of Medicine, University of Leeds, St James’s University Hospital, Leeds, LS9 7TF, UK
  5. Leeds Genetics Laboratories, Leeds Teaching Hospitals NHS Trust, Leeds, LS9 7TF, UK
  6. Northern Genetics Service, Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 3BZ, UK
  7. Department of Cardiology, York Teaching Hospital NHS Foundation Trust, York, YO31 8HE, UK
  8. Institute of Human Genetics, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK
  9. Center for Bioinformatics and Integrative Biology, Faculty of Biological Sciences, Universidad Andrés Bello, Santiago, Chile
  10. Institute of Cardiovascular Sciences, University of Manchester, Manchester, M13 9NT, UK

Corresponding author:
*Dr Rosalyn Jewell
Yorkshire Regional Genetics Service,
3rd Floor, Chapel Allerton Hospital,
Chapel Town Road,
Leeds, LS7 4SA

Email: rosalyn.jewell@nhs.net
Tel: 01133924415
Fax: 01133924434

Journal subject terms:
Arrhythmias, genetics

Key words:
Brugada syndrome, 3p22.2, deletion, SCN5A

Date submitted- 17th August 2018
Date accepted- 12th October 2018