SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE

The Lancet

Volumn 334, Issue 8653, 1989, Pages 52-53

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

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c Department of Paediatrics Streekziekenhuis Helmond Deurne Belgium ^*

^d VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE;

FEMALE; HUMAN; INFANT; LETTER; NEWBORN; PRIORITY JOURNAL; SUDDEN INFANT DEATH SYNDROME;

3-HYDROXYACYL COA DEHYDROGENASES; CASE REPORT; FEMALE; HUMAN; INFANT, NEWBORN; METABOLISM, INBORN ERRORS; MITOCHONDRIA; SUBSTRATE SPECIFICITY; SUDDEN INFANT DEATH;

EID: 0024353075     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(89)90300-0     Document Type: Letter

References (3)

1. Sudden infant death and inherited disorders of fat oxidation
2. Investigation of inborn errors of metabolism in unexpected infant deaths
3. The existence of an inner-membrane-bound, long acyl-chain specific 3-hydroxyacyl-CoA dehydrogenase in mammalian mitochondria