Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy

  • HeartRhythm Case Rep. 2016 Mar 16;2(3):250-254. doi: 10.1016/j.hrcr.2016.02.002.
Marie-A Chaix  1  2 ,  Tamara T Koopmann  3 ,  Philippe Goyette  1 ,  Azadeh Alikashani  1 ,  Frédéric Latour  1 ,  Meena Fatah  3 ,  Robert M Hamilton  3 ,  John D Rioux  1  2
Affiliations
  • 1. Montreal Heart Institute, Montreal, Quebec, Canada.
  • 2. Université de Montréal, Montreal, Quebec, Canada.
  • 3. Physiology and Experimental Medicine, The Hospital for Sick Children & Research Institute, Toronto, Ontario, Canada.
PMID: 28491681 DOI: 10.1016/j.hrcr.2016.02.002
Keywords
CALM3; Calmodulin; Long QT syndrome; Whole exome sequencing.