A novel RyR2 mutation in a 2-year-old baby presenting with atrial fibrillation, atrial flutter, and atrial ectopic tachycardia

Heart Rhythm. 2014 Aug;11(8):1480-3. doi: 10.1016/j.hrthm.2014.04.037. Epub 2014 May 2.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Atrial Fibrillation / genetics*
  • Atrial Fibrillation / metabolism
  • Atrial Fibrillation / physiopathology
  • Atrial Flutter / complications
  • Atrial Flutter / genetics*
  • Atrial Flutter / metabolism
  • Child, Preschool
  • DNA / genetics*
  • DNA Mutational Analysis
  • Electrocardiography
  • Female
  • Follow-Up Studies
  • Humans
  • Mutation*
  • Ryanodine Receptor Calcium Release Channel / genetics*
  • Ryanodine Receptor Calcium Release Channel / metabolism
  • Tachycardia, Ectopic Atrial / complications
  • Tachycardia, Ectopic Atrial / genetics*
  • Tachycardia, Ectopic Atrial / metabolism

Substances

  • Ryanodine Receptor Calcium Release Channel
  • DNA