Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acid β-oxidation

Journal of Inherited Metabolic Disease

Volumn 13, Issue 3, 1990, Pages 311-314

  Wanders, R J A ^a   Ijlst, L ^a   van Gennip, A H ^a   Jakobs, C ^b   de Jager, J P ^c   Dorland, L ^d   van Sprang, F J ^d   Duran, M ^d  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b VU UNIVERSITY AMSTERDAM   (Netherlands)

^c Streekziekenhuis Helmond Deurne ^*  (Netherlands)

^d UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL ENZYME;

CASE REPORT; CONFERENCE PAPER; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FEMALE; HUMAN; INBORN ERROR OF METABOLISM;

3-HYDROXYACYL COA DEHYDROGENASES; CASE REPORT; CELLS, CULTURED; FATTY ACIDS; FEMALE; FIBROBLASTS; HUMAN; INFANT; MITOCHONDRIA; OXIDATION-REDUCTION;

EID: 0025001905     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/BF01799383     Document Type: Article

References (6)

1. The existence of an inner-membrane-bound, long acyl-chain specific 3-hydroxyacyl-CoA dehydrogenase in mammalian mitochondria
2. The presence of a new 3-oxoacyl-CoA thiolase in rat liver perixosomes
3. Purification and properties of mitochondrial and peroxisomal 3-hydroxyacyl-CoA dehydrogenase from rat liver
4. Oxidation of fatty acids
5. The inborn errors of mitochondrial fatty acid oxidation
6. The inborn errors of peroxisomal β-oxidation