A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long QT Syndrome

Ítems similars

• GENETICS OF LONG QT SYNDROME
  per: Tester, David J., et al.
  Publicat: (2014)
• Calmodulin Mutations Associated with Long QT Syndrome Prevent Inactivation of Cardiac L-type Ca(2+) Currents and Promote Proarrhythmic Behavior in Ventricular Myocytes
  per: Limpitikul, Worawan B., et al.
  Publicat: (2014)
• An autism-associated mutation in Ca(V)1.3 channels has opposing effects on voltage- and Ca(2+)-dependent regulation
  per: Limpitikul, Worawan B., et al.
  Publicat: (2016)
• Identification and Functional Characterization of a Novel CACNA1C-Mediated Cardiac Disorder Characterized by Prolonged QT Intervals with Hypertrophic Cardiomyopathy, Congenital Heart Defects, and Sudden Cardiac Death
  per: Boczek, Nicole J., et al.
  Publicat: (2015)
• Novel Gene and Mutation Discovery in Congenital Long QT Syndrome: Let’s Keep Looking Where the Street Lamp Standeth
  per: Tester, David J., et al.
  Publicat: (2008)