'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation

Brain

Volumn 123, Issue 9, 2000, Pages 1896-1902

  Lodi, R ^a,c   Montagna, P ^b   Cortelli, P ^b   Iotti, S ^a   Cevoli, S ^b   Carelli, V ^b   Barbiroli, B ^a  

^a Dipartimento di Medicina Clinica e Biotecnologia Applicata D Campanacci   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Brain and muscle bioenergetics; In vivo metabolism; LHON; MR spectroscopy

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; BRAIN METABOLISM; CLINICAL ARTICLE; ENERGY METABOLISM; FEMALE; GENE MUTATION; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MITOCHONDRIAL RESPIRATION; MUSCLE METABOLISM; OPTIC NERVE DISEASE; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL;

EID: 0033847638     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/123.9.1896     Document Type: Article

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