Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

Eitemau Tebyg

• Potassium channel gene mutations rarely cause atrial fibrillation
  gan: Ellinor, Patrick T, et al.
  Cyhoeddwyd: (2006)
• A Mutation in the S3 Segment of KCNQ1 Results in Familial Lone Atrial Fibrillation
  gan: Das, Saumya, et al.
  Cyhoeddwyd: (2009)
• Genetics of Atrial Fibrillation
  gan: Ellinor, Patrick T., et al.
  Cyhoeddwyd: (2008)
• R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation
  gan: Bartos, Daniel C., et al.
  Cyhoeddwyd: (2010)
• Genetics of Atrial Fibrillation
  gan: Lubitz, Steven A., et al.
  Cyhoeddwyd: (2009)