Fig. 1: Pedigrees of families and identified candidate pathogenic variants in CoQ10 biosynthesis pathway genes.
From: Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype
An arrow indicates the proband. Shaded symbols represent affected individuals. Different shading in family 9 indicates unrelated vision loss (not retinopathy). M – mutant, WT – wildtype.
