SET binding factor 1 (SBF1) mutation causes Charcot-Marie-tooth disease type 4B3

Neurology. 2014 May 6;82(18):1665-6. doi: 10.1212/WNL.0000000000000331.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Charcot-Marie-Tooth Disease / genetics*
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • Mutation, Missense / genetics*
  • Transcriptome / genetics*

Substances

  • Intracellular Signaling Peptides and Proteins