A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance

مواد مشابهة

• Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
  حسب: Carballo, S, وآخرون
  منشور في: (2004)
• Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
  حسب: Carballo, S, وآخرون
  منشور في: (2004)
• Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
  حسب: Carballo, S, وآخرون
  منشور في: (2006)
• Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
  حسب: Carballo, S, وآخرون
  منشور في: (2003)
• Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy
  حسب: Carballo, S, وآخرون
  منشور في: (2005)