Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

相似書籍

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