Evaluation of CACNA1H in European patients with childhood absence epilepsy
Copyright policy )Evaluation of CACNA1H in European patients with childhood absence epilepsy
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.
- University of Helsinki Finland
- Boston Children's Hospital United States
- Assistance Publique -Hopitaux De Paris France
- University Medical Center Groningen Netherlands
- University Medical Center Groningen Netherlands
CALCIUM-CHANNELS, Genotype, Genetic Linkage, T-TYPE, White People, Calcium Channels, T-Type, FUNCTIONAL-CHARACTERIZATION, Asian People, Humans, NEURONS, sequence variants, GENETIC-VARIATION, Chromosome Mapping, ASSOCIATION, DNA, FAMILY, Pedigree, Epilepsy, Absence, childhood absence epilepsy, CACNA1H, SEIZURES, LINKAGE-DISEQUILIBRIUM, linkage, Microsatellite Repeats
CALCIUM-CHANNELS, Genotype, Genetic Linkage, T-TYPE, White People, Calcium Channels, T-Type, FUNCTIONAL-CHARACTERIZATION, Asian People, Humans, NEURONS, sequence variants, GENETIC-VARIATION, Chromosome Mapping, ASSOCIATION, DNA, FAMILY, Pedigree, Epilepsy, Absence, childhood absence epilepsy, CACNA1H, SEIZURES, LINKAGE-DISEQUILIBRIUM, linkage, Microsatellite Repeats
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