Fig. 1From: Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reportsPedigrees of families A and B. Genotypes and sequence profiles are given below each available family member. Exonic sequences are given in capital letters and intronic sequences in small letters, respectively. The nucleotides that are changed are highlighted in red. M, mutant allele; +, wildtype allele; n.a., not analyzedBack to article page