Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban

Registros relacionados

• 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)
• Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
  por: Carballo, S, et al.
  Publicado em: (2004)
• Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
  por: Carballo, S, et al.
  Publicado em: (2006)
• 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)
• Structures of PKA–phospholamban complexes reveal a mechanism of familial dilated cardiomyopathy
  por: Juan Qin, et al.
  Publicado em: (2022-03-01)