Accumulation of deletions and point mutations in mitochondrial genome in degenerative diseases

Annals of the New York Academy of Sciences

Volumn 786, Issue , 1996, Pages 102-111

  Tanaka, Masashi ^a   Kovalenko, Sergey A ^a   Gong, Jian Sheng ^a   Borgeld, Harm Jan W ^a   Katsumata, Kazumi ^a   Hayakawa, Mika ^a   Yoneda, Makoto ^a   Ozawa, Takayuki ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; MITOCHONDRIAL DNA; REACTIVE OXYGEN METABOLITE;

CELL CULTURE; CONFERENCE PAPER; CONTROLLED STUDY; CORPUS STRIATUM; DEGENERATIVE DISEASE; DNA DAMAGE; GENE DELETION; GENOME; GERM LINE; HUMAN; HUMAN TISSUE; LIPID PEROXIDATION; MELAS SYNDROME; MITOCHONDRION; NONSENSE MUTATION; OXIDATIVE STRESS; PARKINSON DISEASE; POINT MUTATION; PROTEIN MODIFICATION; SKELETAL MUSCLE; SOMATIC CELL;

EID: 0029783994     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1996.tb39055.x     Document Type: Conference Paper

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