Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes
Publication year
2019Source
Journal of Inherited Metabolic Disease, 42, 3, (2019), pp. 414-423ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Neurology
Paediatrics
Internal Medicine
Journal title
Journal of Inherited Metabolic Disease
Volume
vol. 42
Issue
iss. 3
Page start
p. 414
Page end
p. 423
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 6: Metabolic Disorders RIHS: Radboud Institute for Health Sciences; Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life SciencesThis item appears in the following Collection(s)
- Academic publications [227437]
- Electronic publications [107154]
- Faculty of Medical Sciences [86157]
- Open Access publications [76295]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.