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