Mitochondrial diseases: Translation matters

Molecular and Cellular Neuroscience

Volumn 55, Issue , 2013, Pages 1-12

  Pearce, Sarah ^a   Nezich, Catherine Laura ^a,b   Spinazzola, Antonella ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

Assembly factors; Mitochondrial encephalopathies; Ribosome; Translation

Indexed keywords

AMINO ACID TRANSFER RNA LIGASE; ELONGATION FACTOR; MESSENGER RNA; MITOCHONDRIAL DNA; RIBOSOME RNA; TRANSFER RNA;

ARTICLE; BRAIN DISEASE; CARDIOMYOPATHY; DIABETES MELLITUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA REPLICATION; DNA TRANSCRIPTION; EXTERNAL OPHTHALMOPLEGIA; GENE MUTATION; HETEROPLASMY; HUMAN; MELAS SYNDROME; MITOCHONDRIAL GENOME; MITOCHONDRIAL MYOPATHY; PERCEPTION DEAFNESS; POLYADENYLATION; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RNA STABILITY; SIDEROBLASTIC ANEMIA;

ANIMALS; GENOME, MITOCHONDRIAL; HUMANS; MITOCHONDRIAL DISEASES; MITOCHONDRIAL PROTEINS; PROTEIN BIOSYNTHESIS;

MAMMALIA;

EID: 84875644184     PISSN: 10447431     EISSN: 10959327     Source Type: Journal    
DOI: 10.1016/j.mcn.2012.08.013     Document Type: Article

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