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ALT positivity in human cancers: prevalence and clinical insights
Genetic Basis and Pathophysiology Most cases of MH are associated with mutations in the RYR1 gene , which encodes the ryanodine receptor type 1 (RyR1) calcium-release channel in skeletal muscle
Public Health 13, 1524399
Gradogna et al
Preliminary Report on Therapeutic Potential of coal-derived Carbon Quantum Dots Against SARS-CoV-2 Virus
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