1998-03-03
Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
Publication
Publication
Proceedings of the National Academy of Sciences of the United States of America , Volume 95 - Issue 5 p. 2128- 2133
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doi.org/10.1073/pnas.95.5.2128, hdl.handle.net/1765/59050 | |
Proceedings of the National Academy of Sciences of the United States of America | |
Organisation | Department of Pediatrics |
van Grunsven, E., van Berkel, E., Ijlst, L., Vreken, P., de Klerk, J., Adamski, J., … Wanders, R. (1998). Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency. In Proceedings of the National Academy of Sciences of the United States of America (Vol. 95, pp. 2128–2133). doi:10.1073/pnas.95.5.2128 |