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
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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
Radboudumc 6: Metabolic Disorders RIHS: Radboud Institute for Health Sciences; Radboudumc 6: Metabolic Disorders RIMLS: Radboud Institute for Molecular Life Sciences; Internal Medicine - Radboud University Medical Center; Radboud University Medical CenterThis item appears in the following Collection(s)
- Academic publications [248471]
- Electronic publications [135730]
- Faculty of Medical Sciences [94202]
- Open Access publications [109003]
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