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