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6. Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene. Gkiourtzis N; Tramma D; Papadopoulou-Legbelou K; Moutafi M; Evangeliou A Am J Med Genet A; 2023 Dec; 191(12):2843-2849. PubMed ID: 37565517 [TBL] [Abstract][Full Text] [Related]
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