NADH-coenzyme Q reductase (complex I) deficiency: Heterogeneity in phenotype and biochemical findings

Journal of Inherited Metabolic Disease

Volumn 19, Issue 5, 1996, Pages 675-686

  Pitkanen S ^a  

^a HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CYTOCHROME C OXIDASE; GALACTOSE; LACTIC ACID; MENADIONE; PYRUVIC ACID; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; BIOCHEMISTRY; CARDIOMYOPATHY; CATARACT; CELL LINE; CLINICAL ARTICLE; CLINICAL FEATURE; COMPARATIVE STUDY; ENZYME ACTIVITY; ENZYME DEFICIENCY; FIBROBLAST CULTURE; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; INFANT; KIDNEY TUBULE DISORDER; LACTIC ACIDEMIA; LACTIC ACIDOSIS; LEIGH DISEASE; LIVER DISEASE; NEWBORN; PHENOTYPE; PRESCHOOL CHILD; SYMPTOM; TOXICITY; TREATMENT OUTCOME;

EID: 0029817733     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799845     Document Type: Article

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