Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression

Overview of attention for article published in Frontiers in Neurology, February 2022

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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

14 Mar 2022

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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

25 Feb 2022

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