A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis

Neuromuscular Disorders

Volumn 14, Issue 2, 2004, Pages 162-166

  McFarland, Robert ^a   Taylor, Robert W ^a   Chinnery, Patrick F ^a   Howell, Neil ^b,c   Turnbull, Douglass M ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b Migenix Inc   (United States)

^c University of Texas Medical Branch School of Medicine   (United States)

Author keywords

Cytochrome c oxidase; DNA sequencing; Mitochondrial DNA; Myoglobinuria; tRNA mutations

Indexed keywords

CYTOCHROME C OXIDASE;

ADULT; ARTICLE; CASE REPORT; DATA BASE; EXERCISE; EXERCISE TOLERANCE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC VARIABILITY; GENOME; HUMAN; MALE; METABOLIC DISORDER; MITOCHONDRION; MYALGIA; MYOGLOBINURIA; PATHOGENICITY; PHENOTYPE; PRIORITY JOURNAL; RHABDOMYOLYSIS;

EID: 0347721039     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2003.10.011     Document Type: Article

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