A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy

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Correspondence to A. Federico.

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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

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Keywords

  • Optic Neuropathy
  • Optic Atrophy
  • Premature Termination Codon
  • Autosomal Dominant Optic Atrophy
  • OPA1 Gene