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Title: Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes
Author(s): Bleeker, Jeannette C.; Kok, Irene L.; Ferdinandusse, Sacha; Pol, W.Ludo van der; Cuppen, Inge ; Bosch, A.M.; Vries, M.C. de ; Rennings, A.J.; Dekkers, E.; Wijburg, Frits A.; Visser, Gepke
Publication year: 2019
Source: Journal of Inherited Metabolic Disease, vol. 42, iss. 3, (2019), pp. 414-423
ISSN: 0141-8955
DOI: https://doi.org/10.1002/jimd.12075
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/203474   http://hdl.handle.net/2066/203474

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Subject: All institutes and research themes of the Radboud University Medical Center
Radboudumc 6: Mitochondrial diseases RIHS: Radboud Institute for Health Sciences
Radboudumc 6: Mitochondrial diseases RIMLS: Radboud Institute for Molecular Life Sciences
Organization: Neurology
Amalia Childrens Hospital
Internal Medicine
Journal title:
Journal of Inherited Metabolic Disease
Volume: vol. 42
Issue: iss. 3
Page start: p. 414
Page end: p. 423

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