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and Group 5, XRI pretreated with melatonin

Conclusion: Approximately 1 in 130 patients with MASLD had genomic evidence for hereditary dyslipidemia (both extremely high and low LDL-C), with rare pathogenic variants in APOB and LDLR being the most common

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131 At present, mitochondrial dynamics have been used to classify tumors, predict clinical prognosis, and therapeutic response

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