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

In the past few years, many patients have been described who have a defect of unknown origin in the peroxisomal beta-oxidation pathway. Complementation analysis has been done by various groups to establish the extent of the genetic heterogeneity among the patients. These studies were based on the us...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: van Grunsven, E G, van Berkel, E, Mooijer, P A, Watkins, P A, Moser, H W, Suzuki, Y, Jiang, L L, Hashimoto, T, Hoefler, G, Adamski, J, Wanders, R J
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 1999
Θέματα:
Research Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377707/
https://ncbi.nlm.nih.gov/pubmed/9915948
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