Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice

Trends Genet. 1999 Apr;15(4):125-8. doi: 10.1016/s0168-9525(99)01716-3.

Abstract

The dosage of the myelin gene and mutant forms of the protein can affect the CNS and PNS. Pelizaeus-Merzbacher disease (PMD) is a myelin disorder of the CNS that arises from both mutational mechanisms. Investigating the molecular basis of PMD in patients and animal models is furthering our understanding of the disease, dosage sensitivity and proteolipid protein function during myelinogenesis.

Publication types

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

MeSH terms

  • Animals
  • Diffuse Cerebral Sclerosis of Schilder / genetics*
  • Gene Duplication
  • Humans
  • Mice
  • Mutation
  • Myelin Proteolipid Protein / genetics*
  • Nerve Degeneration / genetics*
  • Paraplegia / genetics
  • X Chromosome / genetics

Substances

  • Myelin Proteolipid Protein