Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
Những tác giả chính: | Carballo, S, Blair, E, Watkins, H |
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Định dạng: | Conference item |
Được phát hành: |
2004
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Những quyển sách tương tự
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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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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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