Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: A new defect of fatty acid oxidation

Pediatric Research

Volumn 39, Issue 1, 1996, Pages 185-188

  Bennett, Michael J ^a,e   Weinberger, Michael J ^a   Kobori, Joyce A ^b   Rinaldo, Piero ^c   Burlina, Alberto B ^d  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF PADOVA   (Italy)

^e CHILDREN S MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; MITOCHONDRIAL ENZYME; PROMETHAZINE;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FEMALE; FIBROBLAST CULTURE; HUMAN; HUMAN CELL; HYPOGLYCEMIA; KETOACIDOSIS; MALE; PRIORITY JOURNAL; SKIN FIBROBLAST; VOMITING;

EID: 0030041154     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199601000-00031     Document Type: Article

References (14)

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