Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 39, 2007, Pages 15299-15304

  Ling, Jiqiang ^a   Roy, Hervé ^a   Qin, Daoming ^a   Rubio, Mary Anne T ^a   Alfonzo, Juan D ^a   Fredrick, Kurt ^a   Ibba, Michael ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

Aminoacyl tRNA synthetase; Mitochondria; Translation

Indexed keywords

ADENOSINE; INOSINE; MITOCHONDRIAL DNA; PHENYLALANINE TRANSFER RNA; RNA;

AMINOACYLATION; ANTICODON; ARTICLE; BRAIN DISEASE; CONTROLLED STUDY; DIABETES MELLITUS; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; MERRF SYNDROME; MITOCHONDRIAL MYOPATHY; MOLECULAR RECOGNITION; MUTATION; PLEIOTROPY; PRIORITY JOURNAL; PROTEIN FOLDING; RNA STRUCTURE;

ANTICODON; BASE SEQUENCE; EPILEPSIES, MYOCLONIC; HUMANS; KINETICS; MERRF SYNDROME; MITOCHONDRIA; MOLECULAR CONFORMATION; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID CONFORMATION; PEPTIDE ELONGATION FACTOR TU; PHENYLALANINE; RNA; RNA, TRANSFER, PHE;

EID: 34848829840     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0704441104     Document Type: Article

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