CALM3 mutation associated with long QT syndrome

Heart Rhythm. 2015 Feb;12(2):419-22. doi: 10.1016/j.hrthm.2014.10.035. Epub 2014 Oct 31.
No abstract available

Keywords: Arrhythmia; CALM3; Calcium channel inactivation; Calmodulin; Genetics; Long QT syndrome.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • DNA / genetics*
  • DNA Mutational Analysis
  • Electrocardiography*
  • Humans
  • Long QT Syndrome / genetics*
  • Long QT Syndrome / metabolism
  • Long QT Syndrome / physiopathology
  • Male
  • Monomeric Clathrin Assembly Proteins / genetics*
  • Monomeric Clathrin Assembly Proteins / metabolism
  • Mutation*
  • Pedigree

Substances

  • Monomeric Clathrin Assembly Proteins
  • PICALM protein, human
  • DNA