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...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: 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
التنسيق: Artigo
اللغة:Inglês
منشور في: 1999
الموضوعات:
Research Article
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377707/
https://ncbi.nlm.nih.gov/pubmed/9915948
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