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Letter
A novel homozygous change of CLCN2 (p.His590Pro) is associated with a subclinical form of leukoencephalopathy with ataxia (LKPAT)

Authors

  1. Correspondence to Professor Alfredo Brusco, Department of Medical Sciences, University of Torino, via Santena 19, 10126, Torino, Italy; alfredo.brusco{at}unito.it
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Citation

Giorgio E, Vaula G, Benna P, et al
A novel homozygous change of CLCN2 (p.His590Pro) is associated with a subclinical form of leukoencephalopathy with ataxia (LKPAT)

Publication history

  • Received January 11, 2017
  • Revised March 24, 2017
  • Accepted April 3, 2017
  • First published May 4, 2017.
Online issue publication 
February 01, 2018

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