Fig. 3
From: Next generation sequencing technologies for a successful diagnosis in a cold case of Leigh syndrome
IGV visualization (a) and sequence chromatographs (b) of the ECHS1 region flanking the missense mutation c.713C > T/p.Ala238Val from the affected patient (II-1, indicated by an arrow), his father (I-1) and mother (I-2). In IGV the green color corresponds to the nucleotide base A; the brown to the nucleotide base G
