Literature summary for 1.3.8.9 extracted from

Hagemeijer, M.C.; Oussoren, E.; Ruijter, G.J.G.; Onkenhout, W.; Huidekoper, H.H.; Ebberink, M.S.; Waterham, H.R.; Ferdinandusse, S.; de Vries, M.C.; Huigen, M.C.D.G.; Kluijtmans, L.A.J.; Coene, K.L.M.; Blom, H.J.
Abnormal VLCADD newborn screening resembling MADD in four neonates with decreased riboflavin levels and VLCAD activity (2021), JIMD Rep., 61, 12-18 .

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Application

Application	Comment	Organism
diagnostics	maternal riboflavin deficiency in combination with decreased VLCAD activity can result in false-positive VLCADD neonatal screening results with multiple acyl-CoA dehydrogenase deficiency-like biochemistry	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	P49748	-	-

Source Tissue

Source Tissue	Comment	Organism	Textmining
lymphocyte	-	Homo sapiens	-

Synonyms

Synonyms	Comment	Organism
VLCADD	-	Homo sapiens

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Release 2023.1 (January 2023)