A Mutation in the β-Myosin Rod Associated With Hypertrophic Cardiomyopathy Has an Unexpected Molecular Phenotype

Lignende værker

• Mutations in the β-myosin rod cause myosin storage myopathy via multiple mechanisms
  af: Armel, Thomas Z., et al.
  Udgivet: (2009)
• Mutations at the Same Amino Acid in Myosin that Cause Either Skeletal or Cardiac Myopathy Have Distinct Molecular Phenotypes
  af: Armel, Thomas Z., et al.
  Udgivet: (2009)
• Molecular consequences of the R453C hypertrophic cardiomyopathy mutation on human β-cardiac myosin motor function
  af: Sommese, Ruth F., et al.
  Udgivet: (2013)
• The Hypertrophic Cardiomyopathy Myosin Mutation R453C Alters ATP Binding and Hydrolysis of Human Cardiac β-Myosin
  af: Bloemink, Marieke, et al.
  Udgivet: (2014)
• Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
  af: Roopnarine, O, et al.
  Udgivet: (1998)