Fig. 1From: Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysisClinical features of a representative DOA patient, F6-II:2. A fundus images, temporal pallor of the ONH; B OCT, thinning inner retinal neuroepithelial layer, C diffuse thinning of the RNFL. OD, the blue solid line, OS, the purple solid line. D central scotomaBack to article page