Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia

Int J Cardiol. 2015 Apr 15:185:114-6. doi: 10.1016/j.ijcard.2015.03.130. Epub 2015 Mar 11.

¹ Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
² Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
³ National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.
⁴ McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada.
⁵ McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, Canada; Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
⁶ Department of Human Genetics, McGill University, Montreal, Quebec, Canada.
⁷ Toronto General Hospital, Department of Cardiology, University of Toronto, Toronto, Ontario, Canada.
⁸ Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada; Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada. Electronic address: kboycott@cheo.on.ca.
⁹ Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada. Electronic address: rgow@cheo.on.ca.

No abstract available

Keywords: Exome sequencing; Junctional ectopic tachycardia; TNNI3K.

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