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Cardaioli, E., Gallus, G.N., Da Pozzo, P. et al. A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy. J Neurol 253, 672–673 (2006). https://doi.org/10.1007/s00415-005-0057-z
- Optic Neuropathy
- Optic Atrophy
- Premature Termination Codon
- Autosomal Dominant Optic Atrophy
- OPA1 Gene