Revealed a hereditary disease associated with defects in the functioning of the organoid of the cell leading to impaired energy functions in the cells – impaired tissue respiration, synthesis of specific proteins. This disease is transmitted only through the maternal line to children of both sexes. Explain in which organoid the changes took place. Justify the answer.
there was a defect in mitochondrial DNA, incorrect reading of information occurs, the synthesis of specific proteins is disrupted, defects appear in various links of the Krebs cycle, in the respiratory chain, which led to the development of a rare mitochondrial disease.
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