Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation

Lignende værker

• Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
  af: Ritchie, Marylyn D, et al.
  Udgivet: (2012)
• A Common Variant on Chromosome 4q25 is Associated With Prolonged PR Interval in Subjects With and Without Atrial Fibrillation
  af: Kolek, Matthew J., et al.
  Udgivet: (2013)
• Examining Rare and Low-Frequency Genetic Variants Previously Associated with Lone or Familial Forms of Atrial Fibrillation in an Electronic Medical Record System: A Cautionary Note
  af: Weeke, Peter, et al.
  Udgivet: (2014)
• Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation
  af: Parvez, Babar, et al.
  Udgivet: (2012)
• Whole-exome sequencing in familial atrial fibrillation
  af: Weeke, Peter, et al.
  Udgivet: (2014)