Literature summary for 1.5.5.1 extracted from

van der Westhuizen, FH; Smuts, I; Honey, E; Louw, R; Schoonen, M; Jonck, LM; Dercksen, M
A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. (2018), J Neurol Sci, 384, 121-125.

Organism

Organism	UniProt	Comment	Textmining

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Release 2023.1 (January 2023)