Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope

Chin Med J (Engl). 2006 Dec 20;119(24):2129-33.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Death, Sudden, Cardiac / etiology*
  • Female
  • Humans
  • Ion Channels / physiology*
  • Mutation*
  • Ryanodine Receptor Calcium Release Channel / genetics*
  • Syncope / etiology*
  • Tachycardia, Ventricular / genetics*

Substances

  • Ion Channels
  • Ryanodine Receptor Calcium Release Channel