Medical genetics: advances in brief: Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

Ítems similars

• Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.
  per: Straceski, A J, et al.
  Publicat: (1994)
• Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.
  per: Anan, R, et al.
  Publicat: (1994)
• Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
  per: Roopnarine, O, et al.
  Publicat: (1998)
• Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.
  per: Rayment, I, et al.
  Publicat: (1995)
• Hypertrophic Cardiomyopathy Mutations in MYBPC3 Dysregulate Myosin: Implications for Therapy
  per: Toepfer, Christopher N., et al.
  Publicat: (2019)