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Figure 1 | BMC Medical Genetics

Figure 1

From: Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy

Figure 1

Deletions and duplications identified in the OPA1 gene. Black boxes illustrate exons and light grey boxes illustrate alternative spliced exons. Arrows above the gene show the functional domains. Arrows below the gene show localization of deletions identified in the present study (blue arrows) and deletions (green arrows) and duplication (red arrow) identified by Fuhrmann et al. (2009) [23].

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