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Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affected
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  1. Dr EM Wicklein, Department of Neurology, University Hospital Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany.
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Wicklein EM, Orth U, Gal A, et al
Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affected

Publication history

  • Received January 2, 1997
  • Revised April 3, 1997
  • Accepted April 4, 1997
  • First published September 1, 1997.
Online issue publication 
September 01, 1997

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