Oxidative phosphorylation dysfunction does not increase the rate of accumulation of age-related mtDNA deletions in skeletal muscle

Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis

Volumn 379, Issue 1, 1997, Pages 1-11

  Tengan, C H ^a,c   Gabbai, A A ^c   Shanske, S ^d   Zeviani, M ^e   Moraes, C T ^a,b  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MIAMI   (United States)

^c FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^d Columbia University ^*  (United States)

^e BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

AGE; ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON TRANSPORT; GENE DELETION; HUMAN; HUMAN TISSUE; HYPOTHESIS; OXIDATIVE PHOSPHORYLATION; POINT MUTATION; PRIORITY JOURNAL; SKELETAL MUSCLE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AGING; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; EPILEPSIES, MYOCLONIC; FEMALE; GENE DELETION; HUMANS; MALE; MELAS SYNDROME; MIDDLE AGED; MUSCLE, SKELETAL; OXIDATIVE PHOSPHORYLATION; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 0030875420     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0027-5107(97)00076-6     Document Type: Article

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