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

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

Detalhes bibliográficos
Main Authors: Carballo, S, Blair, E, Watkins, H
Formato: Conference item
Publicado em: 2004
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Registos 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)

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