Journal of Neurology

, Volume 253, Issue 5, pp 672–673 | Cite as

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

  • E. Cardaioli
  • G. N. Gallus
  • P. Da Pozzo
  • A. Rufa
  • R. Franceschini
  • E. Motolese
  • A. Caporossi
  • M. T. Dotti
  • A. Federico
LETTER TO THE EDITORS

Keywords

Optic Neuropathy Optic Atrophy Premature Termination Codon Autosomal Dominant Optic Atrophy OPA1 Gene 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

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Copyright information

© Steinkopff-Verlag 2006

Authors and Affiliations

  • E. Cardaioli
    • 1
  • G. N. Gallus
    • 1
  • P. Da Pozzo
    • 1
  • A. Rufa
    • 1
  • R. Franceschini
    • 2
  • E. Motolese
    • 2
  • A. Caporossi
    • 2
  • M. T. Dotti
    • 1
  • A. Federico
    • 1
  1. 1.Department of Neurological and Behavioural SciencesMedical School, University of SienaSienaItaly
  2. 2.Department of Ophthalmological and Neurosurgical SciencesUniversity of SienaSienaItaly

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