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Patients infected with HCV genotypes 2 or 3 have a 70%-80% likelihood of an SVR with a low dose of ribavirin and only 24 weeks of treatment [19, 23, 28 ]

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Concurrent advancements in epigenetic editing and organelle-specific delivery systems can redefine therapeutic precision, enabling spatiotemporal control over lipid metabolic fluxes while minimizing off-target effects associated with conventional enzyme inhibitors

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