Associated Papers
Disorders of riboflavin metabolism.
Balasubramaniam S et al.
Journal of Inherited Metabolic Disease, 2019
Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy.
Auranen M et al.
Neuromuscular Disorders : Nmd, 2017
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.
Olsen RKJ et al.
American Journal of Human Genetics, 2016
Retrograde response to mitochondrial dysfunctions associated to LOF variations in FLAD1 exon 2: unraveling the importance of RFVT2.
Tolomeo M et al.
Free Radical Research, 0
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