A mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain. The disease has characteristics of severe hypertrophic cardi

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déficit combiné de la phosphorylation oxydative type 8

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A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with onset in infancy or early childhood of muscular hypotonia, gait ataxia, mild bilateral pyramidal tract signs, developmental delay (affecting mostly speech and coordi

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déficit combiné de la phosphorylation oxydative type 15

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A rare mitochondrial disease due to a defect in mitochondrial protein synthesis with a variable phenotype that includes onset in infancy or early childhood of failure to thrive and psychomotor regression (after initial normal development), as well as

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déficit combiné de la phosphorylation oxydative type 7

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protein synthesis

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protéosynthèse

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inhibition of protein synthesis

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inhibition de la synthèse des protéines