Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban

Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Carballo, S, Blair, E, Watkins, H
التنسيق:	Conference item
منشور في:	2004

مواد مشابهة

A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
حسب: Carballo, S, وآخرون
منشور في: (2004)

Autosomal dominant HCM and DCM phenotype caused by a novel mutation in phospholamban
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Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
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Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.
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Structures of PKA–phospholamban complexes reveal a mechanism of familial dilated cardiomyopathy
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