Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected]

J Card Fail. 2009 Jun;15(5):464. doi: 10.1016/j.cardfail.2009.04.003.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Aged, 80 and over
  • Amyloidosis / blood
  • Amyloidosis / genetics*
  • Cardiomyopathy, Restrictive / blood
  • Cardiomyopathy, Restrictive / genetics*
  • DNA / genetics*
  • DNA Mutational Analysis
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Mutation*
  • Prealbumin

Substances

  • Prealbumin
  • transthyretin-methionine(111)
  • DNA