Differential occurrence of mutations in mitochondrial DNA of human skeletal muscle during aging

Human Mutation

Volumn 11, Issue 5, 1998, Pages 360-371

  Zhang, Chunfang ^a   Liu, Vincent W S ^a   Addessi, Corrado L ^a   Sheffield, David A ^a   Linnane, Anthony W ^a,b   Nagley, Phillip ^a  

^a MONASH UNIVERSITY   (Australia)

^b AUSTIN HEALTH   (Australia)

Author keywords

Aging; Base substitution; Deletion; mtDNA; Mutation; Skeletal muscle

Indexed keywords

ADENINE; CYTOSINE; GUANINE; MITOCHONDRIAL DNA; THYMINE;

ADOLESCENT; ADULT; AGED; AGING; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DELTOID MUSCLE; GENE DELETION; HUMAN; HUMAN TISSUE; INFANT; NEWBORN; NUCLEIC ACID BASE SUBSTITUTION; ONSET AGE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SKELETAL MUSCLE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AGING; ALLELES; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; HUMANS; INFANT; INFANT, NEWBORN; MIDDLE AGED; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; POINT MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 0031978512     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1998)11:5<360::AID-HUMU3>3.0.CO;2-U     Document Type: Article

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