Literature summary for 1.5.5.1 extracted from

Olsen, RK; Olpin, SE; Andresen, BS; Miedzybrodzka, ZH; Pourfarzam, M; Merinero, B; Frerman, FE; Beresford, MW; Dean, JC; Cornelius, N; Andersen, O; Oldfors, A; Holme, E; Gregersen, N; Turnbull, DM; Morris, AA
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. (2007), Brain, 130, 2045-54.

Organism

Organism	UniProt	Comment	Textmining

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Release 2023.1 (January 2023)