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See Latest ArticlesCardiomyopathy: A Systematic Review of Disease-Causing Mutations in Myosin Heavy Chain 7 and Their Phenotypic Manifestations
Cardiology, 10/28/09
Walsh R et al. – This study suggests that mutation location in the MYH7 gene and changes in amino acid composition can have a negative impact on the disease outcome in individuals with cardiomyopathy.
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Today in Basic Science/Genetics...keeping you current
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Genotype-Phenotype Aspects of Type 2 Long QT Syndrome
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Today in Myocardium/Pericardium...keeping you current
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