Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy Academic Article uri icon

Overview

MeSH Major

  • Cardiomyopathy, Dilated
  • Mutation
  • Troponin T

abstract

  • Thus, the novel cardiac troponin T mutation Arg141Trp is responsible for FDCM in our family. Because several mutations in troponin T have already been recognized to be responsible for FHCM, it appears that the phenotype, whether it be hypertrophy or dilatation, is determined by the specific mutation rather than the gene.

publication date

  • October 30, 2001

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed ID

  • 11684629

Additional Document Info

start page

  • 2188

end page

  • 93

volume

  • 104

number

  • 18