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...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1999
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377707/
https://ncbi.nlm.nih.gov/pubmed/9915948
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