Figure 2From: Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy Pedigrees of three ADOA families A. Family DOA105, B. Family DOA110 C. Family DOA108. Index patients are indicated with an arrow. Filled symbols are individuals affected with ADOA, open symbols are either unaffected or not known. Individuals investigated by deletion analysis are shown with a "+del" (deletion present) or "-del" (no deletion) below symbol.Back to article page