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- W4221074829 abstract "Mitochondria are organelles found in every cell of our body, except for red blood cells, and regulate energy metabolism, apoptosis, and oxidative stress. Proteins controlling these processes are encoded by nuclear or mitochondrial DNA [1]. Mutations in this DNA may result in mitochondrial disease, which are a group of incurable, multi-systemic, and progressive diseases, including mitochondrial depletion syndromes (MDS) [1]. This is a case study on the nutritional management of a patient diagnosed with encephalomyopathic MDS caused by mutations in the nuclear gene RRM2B, required for mitochondrial nucleotide synthesis [2]." @default.
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- W4221074829 date "2022-04-01" @default.
- W4221074829 modified "2023-10-16" @default.
- W4221074829 title "Nutritional management of mitochondrial depletion syndrome: a case study" @default.
- W4221074829 doi "https://doi.org/10.1016/j.clnesp.2022.02.095" @default.
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