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A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy
  1. Dr Maria Muglia, Institute of Neurological Sciences, National Research Council, 87050 Mangone (Cosenza), Italy; m.muglia{at}isn.cnr.it
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Muglia M, Vazza G, Patitucci A, et al
A novel founder mutation in the MFN2 gene associated with variable Charcot–Marie–Tooth type 2 phenotype in two families from Southern Italy

Publication history

  • First published October 16, 2007.
Online issue publication 
October 16, 2007

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