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Mitochondrial Encephalomyopathy and Complex III Deficiency Associated with a Stop-Codon Mutation in the Cytochrome b Gene

Mitochondrial BiogenesisMitochondrial FunctionGenetic DisorderGeneticsInherited Metabolic DiseaseCytochrome B GeneMolecular BiologyMitochondrial MedicineMolecular GeneticsDisease Gene IdentificationMitochondrial EncephalomyopathyMedicineStop-codon Mutation