Literature summary for 1.5.5.1 extracted from

Xi, J; Wen, B; Lin, J; Zhu, W; Luo, S; Zhao, C; Li, D; Lin, P; Lu, J; Yan, C
Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. (2013), J Inherit Metab Dis, , .

Organism

Organism	UniProt	Comment	Textmining

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Release 2023.1 (January 2023)