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A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders

Investigating novel FINs may deepen understanding of ferroptosis-associated disorders and improve the accuracy of LC diagnosis and treatment

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Human blood samples from RA patients, SLE patients, and normal healthy donors and SF samples from RA patients were enrolled from in-patient and physical examination volunteers of West China Hospital, Sichuan University, from May to August 2022

At that point, the mother commented that it seemed like a lot of medicine, and the error was discovered