Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

1998-03-03

Additional Metadata
Persistent URL	doi.org/10.1073/pnas.95.5.2128, hdl.handle.net/1765/59050
Journal	Proceedings of the National Academy of Sciences of the United States of America
Organisation	Department of Pediatrics
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	van Grunsven, E., van Berkel, E., Ijlst, L., Vreken, P., de Klerk, J., Adamski, J., Lemonde, H., Clayton, P., Cuebas, D.& Wanders, R. (1998). Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency. Proceedings of the National Academy of Sciences of the United States of America, 95(5), 2128–2133.https://doi.org/10.1073/pnas.95.5.2128

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