Recognizing Thymidine Kinase 2 Deficiency: A CME Activity on Early Diagnosis of a Rare Mitochondrial Myopathy

This educational activity is designed for European neurologists, pediatricians, medical geneticists, and pulmonologists to improve recognition of thymidine kinase 2 deficiency (TK2d), a rare mitochondrial myopathy. The content emphasizes the urgency of early diagnosis and covers