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Literature summary for 1.5.5.1 extracted from
- Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report. (2018), BMC Med Genomics, 11, 37.
Organism
| Organism | UniProt | Comment | Textmining |
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Release 2023.1 (January 2023)
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