Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI

Int J Cardiol. 2013 Oct 3;168(3):2950-2. doi: 10.1016/j.ijcard.2013.03.168. Epub 2013 Apr 30.
No abstract available

Keywords: Cardiomyopathy; Genetic heart disease; Magnetic resonance imaging; Screening.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cardiac Imaging Techniques*
  • Cardiomyopathy, Hypertrophic / diagnosis*
  • Cardiomyopathy, Hypertrophic / genetics*
  • Carrier Proteins / genetics*
  • Female
  • Humans
  • Isolated Noncompaction of the Ventricular Myocardium / diagnosis*
  • Isolated Noncompaction of the Ventricular Myocardium / genetics*
  • Magnetic Resonance Imaging*
  • Middle Aged
  • Mutation*
  • Young Adult

Substances

  • Carrier Proteins
  • myosin-binding protein C