Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease

Brain. 2012 Aug;135(Pt 8):e217, 1-6; author reply e218, 1-2. doi: 10.1093/brain/aws034. Epub 2012 Mar 1.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Female
  • Hereditary Central Nervous System Demyelinating Diseases / genetics*
  • Humans
  • Male
  • Mutation*
  • Myelin Proteins / genetics*

Substances

  • Myelin Proteins