Evaluation of CACNA1H in European patients with childhood absence epilepsy

Barry Chioza, Kate Everett, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Athanasios Covanis, Olivier Dulac, Martina Durner, Orvar Eeg-Olofsson, Martha Feucht, Mogens Friis, Armin Heils, Marianne Kjeldsen, Katrin Larsson, Anna Elina Lehesjoki, Rima Nabbout, Ingrid Olsson, Thomas Sander, Auli Sirén, Robert RobinsonMichele Rees, R. Mark Gardiner

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

CACNA1H was evaluated in a resource of Caucasian European patients with childhood absence epilepsy by linkage analysis and typing of sequence variants previously identified in Chinese patients. Linkage analysis of 44 pedigrees provided no evidence for a locus in the CACNA1H region and none of the Chinese variants were found in 220 unrelated patients.

Original languageEnglish
Pages (from-to)177-181
Number of pages5
JournalEpilepsy Research
Volume69
Issue number2
DOIs
StatePublished - May 2006
Externally publishedYes

Keywords

  • CACNA1H
  • Childhood absence epilepsy
  • Linkage
  • Sequence variants

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