A Novel RYR2 Loss-of-Function Mutation (I4855M) is Associated with Left Ventricular Non-compaction and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia by Roston, Thomas M., MD, Guo, Wenting, MSc, Krahn, Andrew D., MD, Wang, Ruiwu, PhD, van Petegem, Filip, PhD, Sanatani, Shubhayan, MD, Chen, S.R. Wayne, PhD, Lehman, Anna, MD

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S4153R Is a Gain-of-Function Mutation in the Cardiac Ca2+ Release Channel Ryanodine Receptor Associated With Catecholaminergic Polymorphic Ventricular Tachycardia and Paroxysmal At... by Zhabyeyev, Pavel, PhD, Hiess, Florian, MSc, Wang, Ruiwu, PhD, Liu, Yingjie, MD, Wayne Chen, S.R., PhD, Oudit, Gavin Y., MD, PhD

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