Absence of SCA1 mutation in idiopathic cerebellar ataxia

J Neurol Neurosurg Psychiatry. 1994 Nov;57(11):1439-40. doi: 10.1136/jnnp.57.11.1439-a.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Aged
  • Cerebellar Ataxia / genetics*
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • DNA
  • Diseases in Twins
  • Genetic Carrier Screening
  • Germany
  • Humans
  • Middle Aged
  • Mutagenesis
  • Twins
  • Twins, Monozygotic

Substances

  • DNA