Complementation analysis of carnitine palmitoyltransferase I and II defects

Pediatric Research

Volumn 40, Issue 4, 1996, Pages 542-546

  Slama, A ^a   Brivet, M ^a   Boutron, A ^a   Legrand, A ^a   Saudubray, J M ^b   Demaugre, F ^b  

^a BICÊTRE HOSPITAL   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE PALMITOYLTRANSFERASE; COMPLEMENTARY DNA; LONG CHAIN FATTY ACID;

ADULT; ARTICLE; CARNITINE DEFICIENCY; CONTROLLED STUDY; ENZYME DEFECT; FATTY ACID OXIDATION; FIBROBLAST CULTURE; GENE MUTATION; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; INFANT; MITOCHONDRIAL MEMBRANE; PRIORITY JOURNAL;

EID: 0029785819     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199610000-00005     Document Type: Article

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