A de novo LGI1 mutation in sporadic partial epilepsy with auditory features

Ann Neurol. 2004 Sep;56(3):455-6. doi: 10.1002/ana.20218.
No abstract available

Publication types

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

MeSH terms

  • Codon, Nonsense
  • Epilepsies, Partial / genetics
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Middle Aged
  • Pedigree
  • Proteins / genetics*
  • Seizures / genetics*

Substances

  • Codon, Nonsense
  • Intracellular Signaling Peptides and Proteins
  • LGI1 protein, human
  • Proteins