Autosomal dominant leukodystrophy and childhood ataxia with central nervous system hypomyelination syndrome

Ann Neurol. 2006 Oct;60(4):485; author reply 485-6. doi: 10.1002/ana.20930.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Ataxia / diagnosis*
  • Ataxia / genetics
  • Ataxia / pathology
  • Child
  • Guanine Nucleotide Exchange Factors / physiology
  • Hereditary Central Nervous System Demyelinating Diseases / diagnosis*
  • Hereditary Central Nervous System Demyelinating Diseases / genetics
  • Humans
  • Myelin Sheath / pathology*
  • Syndrome

Substances

  • Guanine Nucleotide Exchange Factors