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Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene

Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsClinical CharacterizationPathologyMolecular BiologyMolecular GeneticsThymidine KinaseMedicineMolecular MedicineMyopathic Form