Mitochondrial disorders have become the most common cause of inborn errors of metabolism. Impairments in mitochondrial protein synthesis are one of the causes of these diseases, which are clinically and genetically heterogeneous. The mitochondrial translation machinery decodes 13 polypeptides essential for the oxidative phosphorylation process. Mitochondria protein synthesis depends on the integrity of mitochondrial rRNAs and tRNAs genes, and at least one hundred of nuclear encoded products. Diseases caused by mutations in mitochondrial genes as well as in ribosomal proteins, translational factors, RNA modifying enzymes, and all other constituents of the translational machinery have been described in patients with combine respiratory chain ...
Mitochondrial protein translation is a complex process performed within mitochondria by an apparatus...
AbstractBy convention, the term “mitochondrial diseases” refers to disorders of the mitochondrial re...
Respiratory chain deficiencies exhibit a wide variety of clinical phenotypes resulting from defectiv...
Mitochondrial disorders have become the most common cause of inborn errors of metabolism. Impairment...
AbstractDefects of the mitochondrial protein synthesis cause a subgroup of mitochondrial diseases, w...
AbstractMitochondrial respiratory chain deficiencies represent one of the major causes of metabolic ...
Mitochondrial respiratory chain (RC) disorders are a group of genetically and clinically heterogeneo...
In eukaryotic cells, mitochondria perform the essential function of producing cellular energy in the...
Diagnosing primary mitochondrial diseases is challenging in clinical practice. Although, defective o...
Mutations in several mitochondrial DNA and nuclear genes involved in mitochondrial protein synthesis...
Diagnosing primary mitochondrial diseases is challenging in clinical practice. Although, defective o...
Mitochondria are one of the most important organelles in cells. Mitochondria are semi-autonomous org...
Mitochondrial disorders are a heterogeneous group of often multisystemic and early fatal diseases, w...
Mutations in several mitochondrial DNA and nuclear genes involved in mitochondrial protein synthesis...
AbstractA strikingly large number of mitochondrial DNA (mtDNA) mutations have been found to be the c...
Mitochondrial protein translation is a complex process performed within mitochondria by an apparatus...
AbstractBy convention, the term “mitochondrial diseases” refers to disorders of the mitochondrial re...
Respiratory chain deficiencies exhibit a wide variety of clinical phenotypes resulting from defectiv...
Mitochondrial disorders have become the most common cause of inborn errors of metabolism. Impairment...
AbstractDefects of the mitochondrial protein synthesis cause a subgroup of mitochondrial diseases, w...
AbstractMitochondrial respiratory chain deficiencies represent one of the major causes of metabolic ...
Mitochondrial respiratory chain (RC) disorders are a group of genetically and clinically heterogeneo...
In eukaryotic cells, mitochondria perform the essential function of producing cellular energy in the...
Diagnosing primary mitochondrial diseases is challenging in clinical practice. Although, defective o...
Mutations in several mitochondrial DNA and nuclear genes involved in mitochondrial protein synthesis...
Diagnosing primary mitochondrial diseases is challenging in clinical practice. Although, defective o...
Mitochondria are one of the most important organelles in cells. Mitochondria are semi-autonomous org...
Mitochondrial disorders are a heterogeneous group of often multisystemic and early fatal diseases, w...
Mutations in several mitochondrial DNA and nuclear genes involved in mitochondrial protein synthesis...
AbstractA strikingly large number of mitochondrial DNA (mtDNA) mutations have been found to be the c...
Mitochondrial protein translation is a complex process performed within mitochondria by an apparatus...
AbstractBy convention, the term “mitochondrial diseases” refers to disorders of the mitochondrial re...
Respiratory chain deficiencies exhibit a wide variety of clinical phenotypes resulting from defectiv...