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This study investigates a 12-year-old patient with mitochondrial encephalomyopathy and hypoparathyroidism, revealing complex mitochondrial DNA (mtDNA) rearrangements including deletions and duplications. The analysis showed that the muscle DNA contained three populations of mtDNA: wild type, deleted (65%), and duplicated (9%). These findings suggest that endocrinopathies other than diabetes can be associated with mtDNA duplications and support the hypothesis that deletions and duplications arise from the sa
- Author
- Haris kokkinis
- Language
- EN