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

E G van Grunsven; E van Berkel; L Ijlst; P Vreken; J B de Klerk; J Adamski; H Lemonde; P T Clayton; D A Cuebas; R J Wanders

doi:10.1073/pnas.95.5.2128

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

Identifier:nobleid.org/w1/20260515/D1FE511B

Type:Conference Paper

0 views

Support unavailableClaim Your Authorship

View Original Paper Source

Embeddable Badge

[![NobleID](https://www.nobleid.org/api/badge/D1FE511B.svg?ark=w1%2F20260515%2FD1FE511B)](https://nobleid.org/work/w1/20260515/D1FE511B)

ARK Inflections

Metadata Policy

Metadata Formats

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors

Claim authorship of this work

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

Identifier:nobleid.org/w1/20260515/D1FE511B

Type:Conference Paper

0 views

Support unavailableClaim Your Authorship

View Original Paper Source

Embeddable Badge

[![NobleID](https://www.nobleid.org/api/badge/D1FE511B.svg?ark=w1%2F20260515%2FD1FE511B)](https://nobleid.org/work/w1/20260515/D1FE511B)

ARK Inflections

Metadata Policy

Metadata Formats

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors

Claim authorship of this work