Absence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):538-9. doi: 10.1002/ajmg.b.30613.
No abstract available

Publication types

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

MeSH terms

  • Basic Helix-Loop-Helix Transcription Factors / genetics*
  • Demyelinating Diseases
  • Humans
  • Motor Neuron Disease
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Oligodendrocyte Transcription Factor 2
  • Pelizaeus-Merzbacher Disease / genetics*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Nerve Tissue Proteins
  • OLIG2 protein, human
  • Oligodendrocyte Transcription Factor 2