Functional analysis of the mutations in the human cardiac beta-myosin that are responsible for familial hypertrophic cardiomyopathy. Implication for the clinical outcome.

Lignende værker

• Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy.
  af: Rayment, I, et al.
  Udgivet: (1995)
• Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.
  af: Anan, R, et al.
  Udgivet: (1994)
• A Novel Mutation of the Beta Myosin Heavy Chain Gene Responsible for Familial Hypertrophic Cardiomyopathy
  af: Wang, Juan, et al.
  Udgivet: (2009)
• Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.
  af: al-Mahdawi, S, et al.
  Udgivet: (1993)
• Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.
  af: Posen, B. M., et al.
  Udgivet: (1995)