Title : Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency.

Pub. Date : 2007 Sep-Oct

PMID : 17689999






1 Functional Relationships(s)
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1 Sequencing of the SLC16A12, RFK and FLAD1 genes encoding key enzymes in riboflavin transport of metabolism in the mother did not identify any pathogenic mutations. Riboflavin flavin adenine dinucleotide synthetase 1 Homo sapiens