Charcot-Marie-Tooth disease type 1 (CMT1) and hereditary neuropathy with liability to pressure palsy (HNPP)

  • E. Nelis
  • P. De Jonghe
  • V. Timmerman


Hereditary Neuropathy Myelin Protein Zero PMP22 Gene Peripheral Myelin Protein Pressure Palsy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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Copyright information

© Steinkopff Verlag Darmstadt 2005

Authors and Affiliations

  • E. Nelis
  • P. De Jonghe
  • V. Timmerman

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