Peroxisomal bifunctional protein deficiency revisited: Resolution of its true enzymatic and molecular basis

American Journal of Human Genetics

Volumn 64, Issue 1, 1999, Pages 99-107

  Van Grunsven, E G ^a   Van Berkel, E ^a   Mooijer, P A W ^a   Watkins, P A ^c   Moser, H W ^c   Suzuki, Y ^d   Jiang, L L ^d   Hashimoto, T ^e   Hoefler, G ^f   Adamski, J ^g   Wanders, R J A ^a,b  

^a Department of Clinical Chemistry   (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d GIFU UNIVERSITY   (Japan)

^e SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f UNIVERSITY OF GRAZ   (Austria)

^g INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; PROTEIN DERIVATIVE;

ARTICLE; CONTROLLED STUDY; FATTY ACID OXIDATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC COMPLEMENTATION; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; PEROXISOME; PRIORITY JOURNAL; PROTEIN DEFICIENCY;

EID: 0033360997     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302180     Document Type: Article

References (12)

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