Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: Clinical, genetic and functional consequences

  • Doolan A
  • Tebo M
  • Ingles J
 et al. 
  • 15

    Readers

    Mendeley users who have this article in their library.
  • 33

    Citations

    Citations of this article.

Abstract

Background. - Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disorder caused by mutations in sarcomeric proteins. Cardiac troponin I (cTnI) is a key switch molecule in the sarcomere. Mutations in cTnI have been identified in

Author-supplied keywords

  • Cardiomyopathy
  • Hypertrophy
  • Interactions
  • Troponin I
  • Troponin complex

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document

Authors

  • Alessandra Doolan

  • Molly Tebo

  • Jodie Ingles

  • Lan Nguyen

  • Tatiana Tsoutsman

  • Lien Lam

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free