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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...

Deskribapen osoa

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:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377707/
https://ncbi.nlm.nih.gov/pubmed/9915948
Etiketak: Etiketa erantsi
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