Nuclear genetic defects of oxidative phosphorylation

Human Molecular Genetics

Volumn 10, Issue 20, 2001, Pages 2277-2284

  Shoubridge, E A ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; OXYGEN; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SUCCINATE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE;

ADULTHOOD; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN DISEASE; CANCER; CELL NUCLEUS; CONTROLLED STUDY; DISEASE ASSOCIATION; FATALITY; GENE DELETION; GENE MUTATION; GENE STRUCTURE; GENETIC CODE; GENETIC DISORDER; GENOTYPE; HEART DISEASE; HUMAN; HYPOXIA; INFANT DISEASE; LIVER DYSFUNCTION; MITOCHONDRION; ONSET AGE; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; PRIORITY JOURNAL; RESPIRATORY CHAIN; REVIEW; STRUCTURAL GENE;

EID: 0035474099     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.20.2277     Document Type: Review

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