Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Antzeko izenburuak

• Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
  nork: Watkins, H, et al.
  Argitaratua: (1993)
• Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.
  nork: Anan, R, et al.
  Argitaratua: (1994)
• Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.
  nork: Watkins, H, et al.
  Argitaratua: (1992)
• Hypertrophic Cardiomyopathy Mutations in MYBPC3 Dysregulate Myosin: Implications for Therapy
  nork: Toepfer, Christopher N., et al.
  Argitaratua: (2019)
• Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.
  nork: Straceski, A J, et al.
  Argitaratua: (1994)