Fig. 1From: New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centreThe percentage of detected MD-related genes, non MD-related genes and non-conclusive WES results in (a) neonates (n = 47), b patients with 3-MGA-uria (n = 16) and c patients with basal ganglia involvement (n = 28)Back to article page