Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with leber's hereditary optic neuropathy

Annals of Neurology

Volumn 45, Issue 3, 1999, Pages 320-328

  Carelli, V ^a,d   Ghelli, A ^a   Bucchi, L ^a   Montagna, P ^a   De Negri, A ^e   Leuzzi, V ^b   Carducci, C ^b   Lenaz, G ^a   Lugaresi, E ^a   Degli Esposti, M ^c  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c MONASH UNIVERSITY   (Australia)

^d UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^e NONE

Author keywords

[No Author keywords available]

Indexed keywords

BENZOQUINONE DERIVATIVE; CYTOCHROME B; DECYLUBIQUINOL; MITOCHONDRIAL DNA; MYXOTHIAZOL; NONYLBENZOQUINOL; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE; UBIQUINONE; UBIQUINONE DERIVATIVE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BIOCHEMISTRY; CLINICAL ARTICLE; CONTROLLED STUDY; DYSTONIA; FEMALE; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; MALE; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL;

ADULT; AMINO ACID SEQUENCE; BLOOD PLATELETS; DNA, MITOCHONDRIAL; FEMALE; FURANS; HUMANS; MALE; METHACRYLATES; MIDDLE AGED; MOLECULAR SEQUENCE DATA; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POINT MUTATION; ROTENONE; THIAZOLES;

EID: 0033028388     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/1531-8249(199903)45:3<320::AID-ANA7>3.0.CO;2-L     Document Type: Article

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