Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy

Registos relacionados

• Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
  Por: Carballo, S, et al.
  Publicado em: (2009)
• Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
  Por: Carballo, S, et al.
  Publicado em: (2004)
• A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
  Por: Carballo, S, et al.
  Publicado em: (2004)
• Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
  Por: Robinson, P, et al.
  Publicado em: (2007)
• Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
  Por: Robinson, P, et al.
  Publicado em: (2003)