Mitochondrial DNA polymorphism in substantia nigra

Journal of the Neurological Sciences

Volumn 144, Issue 1-2, 1996, Pages 204-211

  Kapsa, Robert M I ^a   Jean Francois, M J Bernadette ^a   Lertrit, Patcharee ^a   Weng, Shan ^a   Siregar, Nurjati ^a   Ojaimi, Joseline ^a   Donnan, Geoffrey ^b   Masters, Colin ^c   Byrne, Edward ^a  

^a ST VINCENT S HOSPITAL   (Australia)

^b AUSTIN HOSPITAL   (Australia)

^c UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

complex I; DNA sequencing; long PCR; mitochondrial DNA; mtDNA deletion; mtDNA polymorphism; Parkinson's disease; sequence divergence; substantia nigra

Indexed keywords

MITOCHONDRIAL DNA;

AGED; ARTICLE; CASE REPORT; DNA POLYMORPHISM; DNA SEQUENCE; FEMALE; HUMAN; MALE; PARKINSON DISEASE; PRIORITY JOURNAL; SUBSTANTIA NIGRA;

AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CHROMOSOME DELETION; CONSERVED SEQUENCE; DNA, MITOCHONDRIAL; EVOLUTION, MOLECULAR; FEMALE; HUMANS; MALE; OXYGEN CONSUMPTION; PARKINSON DISEASE; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS; SEQUENCE ANALYSIS, DNA; SUBSTANTIA NIGRA;

EID: 0030449566     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(96)00247-X     Document Type: Article

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