Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.

Ítems similars

• Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function
  per: Sweeney, H. Lee, et al.
  Publicat: (1998)
• Cardiac Troponin Structure-Function and the Influence of Hypertrophic Cardiomyopathy Associated Mutations on Modulation of Contractility
  per: Cheng, Yuanhua, et al.
  Publicat: (2016)
• Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutants
  per: Davis, Jennifer, et al.
  Publicat: (2008)
• Multiple disease genes cause hypertrophic cardiomyopathy
  per: Watkins, Hugh
  Publicat: (1994)
• Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylation()
  per: Messer, Andrew E., et al.
  Publicat: (2016)