Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
Үндсэн зохиолчид: | Carballo, S, Blair, E, Watkins, H |
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Формат: | Conference item |
Хэвлэсэн: |
2004
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
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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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