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A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix-Saguenay
  1. Correspondence to:
 Dr Satoshi Okawa
 Department of Neurology, Akita University School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan; sato{at}doc.med.akita-u.ac.jp
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Okawa S, Sugawara M, Watanabe S, et al
A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix-Saguenay

Publication history

  • First published January 17, 2006.
Online issue publication 
January 17, 2006

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