Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
Autors principals: | Carballo, S, Redwood, C, Robinson, P, Blair, E, Watkins, H |
---|---|
Format: | Conference item |
Publicat: |
2006
|
Ítems similars
-
Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
per: Carballo, S, et al.
Publicat: (2009) -
Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
per: Carballo, S, et al.
Publicat: (2004) -
A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
per: Carballo, S, et al.
Publicat: (2004) -
Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
per: Robinson, P, et al.
Publicat: (2007) -
Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
per: Robinson, P, et al.
Publicat: (2003)