Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of d-Bifunctional Protein

In this report, we reinvestigate the only patient ever reported with a deficiency of peroxisomal 3-ketoacyl-CoA thiolase (THIO). At the time when they were described, the abnormalities in this patient, which included accumulation of very-long-chain fatty acids and the bile-acid intermediate trihydro...

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Autors principals: Ferdinandusse, S., van Grunsven, E. G., Oostheim, W., Denis, S., Hogenhout, E. M., IJlst, L., van Roermund, C. W. T., Waterham, H. R., Goldfischer, S., Wanders, R. J. A.
Format: Artigo
Idioma:Inglês
Publicat: The American Society of Human Genetics 2002
Matèries:
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC379147/
https://ncbi.nlm.nih.gov/pubmed/11992265
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