Characterization of the human mitochondrial aconitase gene (ACO2)

Gene

Volumn 213, Issue 1-2, 1998, Pages 205-218

  Mirel, Daniel B ^a   Marder, Karen ^b   Graziano, Joseph ^c   Freyer, Greg ^c   Zhao, Qiuqu ^c   Mayeux, Richard ^b   Wilhelmsen, Kirk C ^a  

^a UNIVERSITY OF CALIFORNIA SAN FRANCISCO   (United States)

^b Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^c Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

Intermediary metabolism; Linkage disequilibrium; Parkinson's disease; Single nucleotide polymorphism

Indexed keywords

ACONITATE HYDRATASE; ALLOENZYME; DNA; IRON; MITOCHONDRIAL ENZYME;

ALLELE; ARTICLE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; DNA TRANSCRIPTION; ENERGY METABOLISM; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; IRON METABOLISM; MAJOR CLINICAL STUDY; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PARKINSON DISEASE; PRIORITY JOURNAL;

ACONITATE HYDRATASE; ALLELES; AMINO ACID SEQUENCE; BASE SEQUENCE; BLOTTING, WESTERN; CHROMOSOMES, HUMAN, PAIR 22; CLONING, MOLECULAR; DNA, COMPLEMENTARY; EXONS; GENE EXPRESSION REGULATION; GENES; HUMANS; IRON; ISOELECTRIC FOCUSING; ISOENZYMES; LINKAGE DISEQUILIBRIUM; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; PARKINSON DISEASE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SUBSTANTIA NIGRA;

EID: 0032525985     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00188-7     Document Type: Article

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