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Mutations in the genes required for the biosynthesis of CoQ 10 lead to primary CoQ 10 deficiency (PCD) and present with heterogeneous clinical symptoms ranging from birth- or infantile-onset multisystem disorders to isolated symptoms involving single organs or systems
But its origin hints at its incredible function: protection and repair
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The LPO process highlights ACSL4, LPCAT3, and LOXs as important targets for regulating ferroptosis
Structural and metabolic changes in Atp7b/ mouse liver and potential for new interventions in Wilsons disease
