Literature summary for 1.5.5.1 extracted from

Chautard, R; Laroche-Raynaud, C; Lia, AS; Chazelas, P; Derouault, P; Sturtz, F; Baaj, Y; Veauville-Merlli�, A; Acquaviva, C; Favreau, F; Faye, PA
A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene. (2020), BMC Med Genomics, 13, 12.

Organism

Organism	UniProt	Comment	Textmining

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Release 2023.1 (January 2023)