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

Benzer Materyaller

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