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HeartRhythm Case Reports
(May 2016)
Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
Marie-A. Chaix, MD, MSc,
Tamara T. Koopmann, PhD,
Philippe Goyette, PhD,
Azadeh Alikashani, MSc,
Frédéric Latour, MSc,
Meena Fatah, HBSc,
Robert M. Hamilton, MD,
John D. Rioux, PhD
Affiliations
Marie-A. Chaix, MD, MSc
Montreal Heart Institute, Montreal, Quebec, Canada
Tamara T. Koopmann, PhD
Physiology and Experimental Medicine, The Hospital for Sick Children & Research Institute, Toronto, Ontario, Canada
Philippe Goyette, PhD
Montreal Heart Institute, Montreal, Quebec, Canada
Azadeh Alikashani, MSc
Montreal Heart Institute, Montreal, Quebec, Canada
Frédéric Latour, MSc
Montreal Heart Institute, Montreal, Quebec, Canada
Meena Fatah, HBSc
Physiology and Experimental Medicine, The Hospital for Sick Children & Research Institute, Toronto, Ontario, Canada
Robert M. Hamilton, MD
Physiology and Experimental Medicine, The Hospital for Sick Children & Research Institute, Toronto, Ontario, Canada
John D. Rioux, PhD
Montreal Heart Institute, Montreal, Quebec, Canada
DOI
https://doi.org/10.1016/j.hrcr.2016.02.002
Journal volume & issue
Vol. 2, no. 3
pp. 250 – 254
Abstract
Read online
No abstracts available.
Keywords
Long QT syndrome
Calmodulin
CALM3
Whole exome sequencing
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