A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
Päätekijät: | Carballo, S, Blair, E, Watkins, H |
---|---|
Aineistotyyppi: | Conference item |
Julkaistu: |
2004
|
Samankaltaisia teoksia
-
Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
Tekijä: Carballo, S, et al.
Julkaistu: (2004) -
Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
Tekijä: Carballo, S, et al.
Julkaistu: (2004) -
Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
Tekijä: Carballo, S, et al.
Julkaistu: (2006) -
Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
Tekijä: Carballo, S, et al.
Julkaistu: (2003) -
Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy
Tekijä: Carballo, S, et al.
Julkaistu: (2005)