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11. Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro Characterization. (1st September 2021)

12. Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro Characterization. (September 2021)

13. Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?. (August 2017)

14. Management of Congenital Long-QT Syndrome: Commentary From the Experts. (9th July 2021)

15. Management of Congenital Long-QT Syndrome: Commentary From the Experts. (July 2021)

17. Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome. (February 2017)