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

Gelijkaardige items

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