EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.5.5.1 | acyl-coa dehydrogenase deficiency |
19265687 |
Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. |
causal interaction
unassigned |
3
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
19774399 |
Characterizing the transcriptional regulation of let-721, a Caenorhabditis elegans homolog of human electron flavoprotein dehydrogenase. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
20138856 |
High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. |
causal interaction
unassigned |
2
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
20392676 |
In vitro probe acylcarnitine profiling assay using cultured fibroblasts and electrospray ionization tandem mass spectrometry predicts severity of patients with glutaric aciduria type 2. |
causal interaction
unassigned |
4
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
20674745 |
Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency. |
unassigned |
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
20937244 |
The electron transfer flavoprotein: Ubiquinone oxidoreductases. |
unassigned |
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
21596162 |
Characterization of mitochondrial proteome in a severe case of ETF-QO deficiency. |
causal interaction
ongoing research
unassigned |
4
2
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
22190129 |
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect. |
causal interaction
unassigned |
2
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
23106979 |
A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene. |
causal interaction
unassigned |
2
0 |
| 1.5.5.1 | acyl-coa dehydrogenase deficiency |
24357026 |
Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
