Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.

Παρόμοια τεκμήρια

• Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.
  ανά: Cuda, G, κ.ά.
  Έκδοση: (1993)
• Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
  ανά: Lankford, E B, κ.ά.
  Έκδοση: (1995)
• Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.
  ανά: Anan, R, κ.ά.
  Έκδοση: (1994)
• Functional analysis of the mutations in the human cardiac beta-myosin that are responsible for familial hypertrophic cardiomyopathy. Implication for the clinical outcome.
  ανά: Sata, M, κ.ά.
  Έκδοση: (1996)
• Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
  ανά: Fananapazir, L, κ.ά.
  Έκδοση: (1993)