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

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

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  • Alessandra Doolan

  • Molly Tebo

  • Jodie Ingles

  • Lan Nguyen

  • Tatiana Tsoutsman

  • Lien Lam

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