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

Podobne zapisy

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