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pro vyhledávání: '"Paul Vanden Broucke"'
Autor:
Toon Van Genechten, François Eyskens, Paul Vanden Broucke, Geert Smits, Sam Proesmans, Viviane Van Hoof, Seppe vanden Broucke, Kristien Wouters, Elke Smits, Tim Van den Bulcke
Publikováno v:
Journal of biomedical informatics
Newborn screening programs for severe metabolic disorders using tandem mass spectrometry are widely used. Medium-Chain Acyl-CoA dehydrogenase deficiency (MCADD) is the most prevalent mitochondrial fatty acid oxidation defect (1:15,000 newborns) and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::833c51af3c6a476371d938f6bee791df
