Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 5, 1998, Pages 2128-2133

  Van Grunsven, Elisabeth G ^a   Van Berkel, Emanuel ^a   Ijlst, Lodewijk ^a   Vreken, Peter ^a   De Klerk, Johannis B C ^b   Adamski, Jerzy ^c   Lemonde, Hugh ^d   Clayton, Peter T ^d   Cuebas, Dean A ^e   Wanders, Ronald J A ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b SOPHIA CHILDREN S HOSPITAL   (Netherlands)

^c INSTITUTE OF EPIDEMIOLOGY   (Germany)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e MISSOURI STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ENOYL COENZYME A HYDRATASE;

CASE REPORT; CONFERENCE PAPER; ENZYME DEFECT; FATTY ACID OXIDATION; GENE MUTATION; HUMAN; HUMAN CELL; MALE; PEROXISOME; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN FIBROBLAST;

EID: 13144277564     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.5.2128     Document Type: Article

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