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C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndrome

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References

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Correspondence to Giuliana Galassi.

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Galassi, G., Maggi, L., Lamantea, E. et al. C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndrome. Acta Neurol Belg 117, 947–949 (2017). https://doi.org/10.1007/s13760-017-0793-8

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  • DOI: https://doi.org/10.1007/s13760-017-0793-8

Keywords

  • Multiple Sclerosis
  • Mitochondrial Disorder
  • Clinically Isolate Syndrome
  • C10ORF2 Mutation
  • C10ORF2 Gene