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Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy by 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
Published 2016-05-01
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