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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 August 11, 2012
  • Revised September 27, 2012
  • Accepted October 5, 2012
  • First published November 27, 2012.

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