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dc.contributor.authorJager, Emmalie A
dc.contributor.authorKuijpers, Myrthe M
dc.contributor.authorBosch, Annet M
dc.contributor.authorMulder, Margot F
dc.contributor.authorGozalbo, Estela R
dc.contributor.authorVisser, Gepke
dc.contributor.authorde Vries, Maaike
dc.contributor.authorWilliams, Monique
dc.contributor.authorWaterham, Hans R
dc.contributor.authorvan Spronsen, Francjan J
dc.contributor.authorSchielen, Peter C J I
dc.contributor.authorDerks, Terry G J
dc.date.accessioned2019-10-23T15:42:21Z
dc.date.available2019-10-23T15:42:21Z
dc.date.issued2019-09-01
dc.identifier.issn1573-2665
dc.identifier.pmid31012112
dc.identifier.doi10.1002/jimd.12102
dc.identifier.urihttp://hdl.handle.net/10029/623418
dc.language.isoenen_US
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectacylcarnitineen_US
dc.subjectinborn errors of metabolismen_US
dc.subjectmedium-chain acyl-CoA dehydrogenase deficiencyen_US
dc.subjectneonatal screeningen_US
dc.subjectprevalenceen_US
dc.titleA nationwide retrospective observational study of population newborn screening for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in the Netherlands.en_US
dc.typeArticleen_US
dc.identifier.journalJ Inherit Metab Dis 2019; advance online publication (ahead of print)en_US
dc.source.journaltitleJournal of inherited metabolic disease


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