This chapter provides a comprehensive review of the genomic and epigenetic underpinnings of major cardiovascular diseases, including coronary artery disease, cardiomyopathies, and hereditary arrhythmia syndromes. It critically examines findings from genome-wide association studies, whole-exome sequencing, and single-cell transcriptomics, while highlighting the emerging roles of DNA methylation, histone modification, and non-coding RNAs in cardiac pathophysiology. The chapter further explores how molecular insights are being translated into precision medicine strategies and novel therapeutic targets.

Medical Science
Genomics, Epigenetics, and Molecular Mechanisms of Cardiovascular Disease
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