Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy
Author:
Affiliation:
1. Department of Pediatrics, Hospital for Sick Children, Toronto, Ontario, Canada (L.Z., R.Y., S.M.).
2. Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada (M.T.).
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference5 articles.
1. Spectrum and Prevalence of CALM1 -, CALM2 -, and CALM3 -Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome–Associated Calmodulin Missense Variant, E141G
2. Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility
3. Calmodulin Mutations Associated With Recurrent Cardiac Arrest in Infants
4. Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes
5. Investigation into the promoter DNA methylation of three genes (CAMK1D, CRY2 and CALM2) in the peripheral blood of patients with type 2 diabetes
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