The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel

Gelijkaardige items

• Author's reply: link of SCN5A SNP R1193Q to long QT syndrome
  door: Wang, Q
  Gepubliceerd in: (2005)
• R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese
  door: Hwang, H, et al.
  Gepubliceerd in: (2005)
• “Pill-in-the-Pocket” Treatment of Propafenone Unmasks ECG Brugada Pattern in an Atrial Fibrillation Patient With a Common SCN5A R1193Q Polymorphism
  door: Linling Li, et al.
  Gepubliceerd in: (2019-03-01)
• “Pill-in-the-Pocket” Treatment of Propafenone Unmasks ECG Brugada Pattern in an Atrial Fibrillation Patient With a Common SCN5A R1193Q Polymorphism
  door: Li, Linling, et al.
  Gepubliceerd in: (2019)
• Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy
  door: Rossenbacker, T, et al.
  Gepubliceerd in: (2005)