Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

Journal of Inherited Metabolic Disease

Volumn 20, Issue 5, 1997, Pages 674-680

  Marin Garcia, J ^a  

^a Molecular Cardiology Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; CASE REPORT; CHILD; ENZYME ACTIVITY; ENZYME DEFECT; FEMALE; HEART MITOCHONDRION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INFANT; MALE; MITOCHONDRIAL RESPIRATION; NEWBORN; POINT MUTATION; PRESCHOOL CHILD;

CARDIOMYOPATHY, HYPERTROPHIC; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; GENE DELETION; HUMANS; INFANT; INFANT, NEWBORN; MALE; MITOCHONDRIA, HEART; MUTATION;

EID: 0030821822     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005322409330     Document Type: Article

References (15)

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