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Journal ArticleOPEN ACCESS

Triadin mutations - a cause of ventricular arrhythmias in children and young adults

  • Hancox J
  • James A
  • Walsh M
  • et al.
Journal of Congenital Cardiology (2017) 1(1)
DOI: 10.1186/s40949-017-0011-9
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Abstract

Triadin-1, encoded by TRDN, is an important component of the calcium release unit (CRU) in the sarcoplasmic reticulum of cardiac myocytes, interacting both with ryanodine receptors and calsequestrin. This article reviews evidence substantiating a link between TRDN mutations and potentially fatal ventricular arrhythmias.

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Hancox, J. C., James, A. F., Walsh, M. A., & Stuart, A. G. (2017). Triadin mutations - a cause of ventricular arrhythmias in children and young adults. Journal of Congenital Cardiology, 1(1). https://doi.org/10.1186/s40949-017-0011-9

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