Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. Hum Mol Genet. 2012 May 01; 21(9):2039-53.
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Animals
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Animals, Newborn
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Cardiomyopathy, Dilated
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Cardiomyopathy, Hypertrophic, Familial
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Case-Control Studies
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Codon, Nonsense
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Female
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Humans
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Male
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Mice
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Mice, Inbred C57BL
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Mice, Transgenic
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Microscopy, Electron, Transmission
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Muscle Proteins
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Mutant Proteins
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Mutation
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Mutation, Missense
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Myocardium
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Myocytes, Cardiac
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Nuclear Proteins
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Pedigree
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Phenotype
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Protein Binding
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Rats
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Rats, Mutant Strains
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Rats, Sprague-Dawley
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Repressor Proteins