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