Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.

Lignende værker

• Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
  af: Roopnarine, O, et al.
  Udgivet: (1998)
• Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
  af: Solomon, S D, et al.
  Udgivet: (1990)
• Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
  af: Watkins, H, et al.
  Udgivet: (1992)
• Medical genetics: advances in brief: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
  af: Norman, Andrew
  Udgivet: (1992)
• Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function
  af: Schmitt, Joachim P., et al.
  Udgivet: (2006)