Fig. 2From: Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases reportThe chromatogram of ETFDH variants. The compound heterozygous mutations c.34G > C and c.1211 T > C in case 1 (a), and compound heterozygous mutations c.736G > A and c.1454C > G in case 2 (b)Back to article page