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Evaluation of CACNA1H in European patients with childhood absence epilepsy

Item Type:Article
Title:Evaluation of CACNA1H in European patients with childhood absence epilepsy
Creators Name:Chioza, B. and Everett, K. and Aschauer, H. and Brouwer, O. and Callenbach, P. and Covanis, A. and Dulac, O. and Durner, M. and Eeg-Olofsson, O. and Feucht, M. and Friis, M. and Heils, A. and Kjeldsen, M. and Larsson, K. and Lehesjoki, A.E. and Nabbout, R. and Olsson, I. and Sander, T. and Siren, A. and Robinson, R. and Rees, M. and Gardiner, R.M.
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.
Keywords:Childhood absence epilepsy, CACNA1H, Linkage, Sequence variants
Source:Epilepsy Research
Page Range:177-181
Date:May 2006
Official Publication:https://doi.org/10.1016/j.eplepsyres.2006.01.009
PubMed:View item in PubMed

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