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The increased biogenesis resulted in a delayed development of morphological hallmarks, ultrastructural abnormalities, and the prevention of mtDNA deletion accumulation in skeletal muscle
However, the relevance of these findings will certainly be reinforced if T1D-MVPs exist at birth and, if so, will support the possibility of a stochastic or environmental factor that takes effect in utero
Following absorption in the gut, TMA enters the bloodstream and travels through the gastrointestinal lining before being processed by the liver [12]
Lubbe, L., Cozier, G
