Human diseases with impaired mitochondrial protein synthesis

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1807, Issue 9, 2011, Pages 1198-1205

  Rötig, Agnès ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Genetic disease; Mitochondria; Translation

Indexed keywords

AMINO ACID TRANSFER RNA LIGASE; CYTOCHROME C; CYTOCHROME C OXIDASE; ELONGATION FACTOR; MESSENGER RNA; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN; PROTEIN C12ORF65; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RIBOSOME PROTEIN; RIBOSOME RNA; RNA 12S; RNA 16S; SUCCINATE DEHYDROGENASE (UBIQUINONE); TRANSFER RNA; UBIQUINOL CYTOCHROME C REDUCTASE; UNCLASSIFIED DRUG;

ARTICLE; CELL DIVISION; CLINICAL FEATURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA STRUCTURE; EXOME; FRAMESHIFT MUTATION; GENE DELETION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPERURICEMIA PULMONARY HYPERTENSION RENAL FAILURE AND ALKALOSIS SYNDROME; MELAS SYNDROME; MISSENSE MUTATION; MITOCHONDRIAL GENOME; MITOCHONDRIAL PROTEIN SYNTHESIS DEFICIENCY; PATHOGENICITY; PERRAULT SYNDROME; PONTOCEREBELLAR HYPOPLASIA; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RESPIRATORY CHAIN; RNA STABILITY; RNA TRANSLATION; SPLICING DEFECT;

DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; HUMANS; METABOLIC DISEASES; MITOCHONDRIA; PROTEIN BIOSYNTHESIS;

EID: 79960555933     PISSN: 00052728     EISSN: 18792650     Source Type: Journal    
DOI: 10.1016/j.bbabio.2011.06.010     Document Type: Review

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