Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

Molecular and Cellular Biology

Volumn 12, Issue 2, 1992, Pages 480-490

  King, M P ^a   Koga, Y ^a   Davidson, M ^a   Schon, E A ^a  

^a Columbia University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BRAIN DISEASE; CASE REPORT; FEMALE; HUMAN; HUMAN CELL; LACTIC ACIDOSIS; MELAS SYNDROME; MITOCHONDRIAL MYOPATHY; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RESPIRATORY CHAIN;

EID: 0026573082     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.12.2.480     Document Type: Article

References (0)