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Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression https://t.co/45K6tFE5Pv https://t.co/gLF4YKLlT9
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression https://t.co/45K6tFE5Pv https://t.co/gLF4YKLlT9
New Research: Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression: The nuclear gene TK2 encodes the mitochondrial thymidine kinase, an enzyme… https://t.co/W59vC