Mitochondria in neuromuscular disorders

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1366, Issue 1-2, 1998, Pages 199-210

  Dimauro, Salvatore ^a   Bonilla, Eduardo ^a   Davidson, Mercy ^a   Hirano, Michio ^a   Schon, Eric A ^a,b  

^a P and S 4 420   (United States)

^b New York Presbyterian Columbia University Medical Center   (United States)

Author keywords

Coenzyme Q10 deficiency; Cytochrome c oxidase deficiency; Defects of mtDNA; Mitochondrial encephalomyopathy; Mitochondrial genetics

Indexed keywords

CARRIER PROTEIN; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; STRUCTURAL PROTEIN; UBIDECARENONE;

ENCEPHALOMYOPATHY; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENE REARRANGEMENT; HEREDITARY OPTIC ATROPHY; HUMAN; LEIGH DISEASE; MITOCHONDRION; NEUROMUSCULAR DISEASE; PATHOGENESIS; POINT MUTATION; PRIORITY JOURNAL; RESPIRATORY CHAIN; REVIEW;

EID: 0032504656     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0005-2728(98)00113-3     Document Type: Article

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