Evaluation of CACNA1H in European patients with childhood absence epilepsy

Tools

Item Type:	Article
Title:	Evaluation of CACNA1H in European patients with childhood absence epilepsy
Creators Name:	Chioza, B., Everett, K., Aschauer, H., Brouwer, O., Callenbach, P., Covanis, A., Dulac, O., Durner, M., Eeg-Olofsson, O., Feucht, M., Friis, M., Heils, A., Kjeldsen, M., Larsson, K., Lehesjoki, A.E., Nabbout, R., Olsson, I., Sander, T., Siren, A., Robinson, R., 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
ISSN:	0920-1211
Publisher:	Elsevier
Volume:	69
Number:	2
Page Range:	177-181
Date:	May 2006
Official Publication:	https://doi.org/10.1016/j.eplepsyres.2006.01.009
PubMed:	View item in PubMed

Repository Staff Only: item control page