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A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

Authors

  1. Correspondence to Dr Yoshihisa Takiyama, Department of Neurology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Chuo-shi, Yamanashi 409-3898, Japan; ytakiyama{at}yamanashi.ac.jp
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Citation

Shimazaki H, Takiyama Y, Ishiura H, et al
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

Publication history

  • Received 11 August 2012
  • Revised 27 September 2012
  • Accepted 5 October 2012
  • Published in print 1 December 2012.
  • Published online 27 November 2012.

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