A novel deletion mutation in the cardiac myosin-binding protein C gene as a cause of Maron's type IV hypertrophic cardiomyopathy

Am J Cardiol. 2002 Feb 15;89(4):487-8. doi: 10.1016/s0002-9149(01)02281-0.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Cardiomyopathy, Hypertrophic / genetics*
  • Carrier Proteins / genetics*
  • Female
  • Gene Deletion*
  • Humans
  • Myosins / genetics*
  • Sequence Analysis, DNA

Substances

  • Carrier Proteins
  • myosin-binding protein C
  • Myosins