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Kalpana Vijayan

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Open access 2026

Multi-omic analysis identifies mitochondrial dysfunction as a key feature of hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is an inherited cardiovascular disorder marked by left ventricular hypertrophy, known to be caused by genetic mutations in sarcomere proteins, such as MYH7 and MYBPC3. Despite advancements in our understanding of HCM genetics, the relationship between genetic variants and clinical outc...

Aryan Velu, Kalpana Vijayan · 0 citations

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