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A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia
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  1. Correspondence to:
 Dr C Goizet
 Service de Neurologie, CHU Pellegrin, Place Amélie Raba-Léon, F-33076 Bordeaux Cedex, France; cyril.goizetchu-bordeaux.fr
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Citation

Goizet C, Ben Yaou R, Demay L, et al
A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia

Publication history

  • Received October 7, 2003
  • Accepted October 14, 2003
  • First published March 1, 2004.
Online issue publication 
March 01, 2004

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