Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
Main Authors: | Carballo, S, Blair, E, Watkins, H |
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Format: | Conference item |
Udgivet: |
2004
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Lignende værker
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A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
af: Carballo, S, et al.
Udgivet: (2004) -
Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
af: Carballo, S, et al.
Udgivet: (2004) -
Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
af: Carballo, S, et al.
Udgivet: (2006) -
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
af: Carballo, S, et al.
Udgivet: (2009) -
Structures of PKA–phospholamban complexes reveal a mechanism of familial dilated cardiomyopathy
af: Juan Qin, et al.
Udgivet: (2022-03-01)