Phenotype variability in a caucasian family with dentatorubral-pallidoluysian atrophy

Eur Neurol. 2004;52(3):175-6. doi: 10.1159/000081859. Epub 2004 Nov 2.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Family Health
  • Female
  • Genetic Variation / genetics*
  • Humans
  • Myoclonic Epilepsies, Progressive / genetics*
  • Phenotype*
  • Trinucleotide Repeats / genetics
  • White People / genetics*