Associated Papers
Copy number amplification of FLAD1 promotes the progression of triple-negative breast cancer through lipid metabolism.
Song XQ et al.
Nature Communications, 2025
39890808 (PubMed )
Supplement: 41467_2025_56458_MOESM3_ESM.pdf
A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene.
Wen B et al.
Journal of Human Genetics, 2024
Why Don't More Mitochondrial Diseases Exhibit Cardiomyopathy?
Singh N et al.
Journal of Cardiovascular Development and Disease, 2023
37103033 (PubMed )
Supplement: jcdd-10-00154-s001.zip › Table_S1.xlsx › GeneData
Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: a single-center retrospective study.
Wen B et al.
Human Molecular Genetics, 2022
FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening.
Muru K et al.
Molecular Genetics & Genomic Medicine, 2019
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
Mutation Spectrum of Primary Lipid Storage Myopathies.
Vengalil S et al.
Annals of Indian Academy of Neurology, 0
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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