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Evaluation of CACNA1H in European patients with childhood absence epilepsy
- Chioza, B. (author)
- Everett, K. (author)
- Aschauer, H. (author)
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- Brouwer, O. (author)
- Callenbach, P. (author)
- Covanis, A. (author)
- Dulac, O. (author)
- Durner, M. (author)
- Feucht, M. (author)
- Friis, M. (author)
- Heils, A. (author)
- Kjeldsen, M. (author)
- Lehesjoki, A. E. (author)
- Nabbout, R. (author)
- Sander, T. (author)
- Siren, A. (author)
- Robinson, R. (author)
- Rees, M. (author)
- Gardiner, R. M. (author)
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- (creator_code:org_t)
- Elsevier BV, 2006
- 2006
- English.
- In: Epilepsy Res. - : Elsevier BV. - 0920-1211. ; 69:2, s. 177-81
- Journal article (peer-reviewed)
Abstract
Subject headings
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- 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.
Keyword
- Asian Continental Ancestry Group/*genetics
- Calcium Channels
- T-Type/*genetics
- Chromosome Mapping
- DNA/genetics
- Epilepsy
- Absence/*genetics
- European Continental Ancestry Group/*genetics
- Genotype
- Humans
- *Linkage (Genetics)
- Microsatellite Repeats
- Pedigree
- Asian Continental Ancestry Group/*genetics
Publication and Content Type
- ref (subject category)
- art (subject category)
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- By the author/editor
- Chioza, B.
- Everett, K.
- Aschauer, H.
- Brouwer, O.
- Callenbach, P.
- Covanis, A.
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- Dulac, O.
- Durner, M.
- Eeg-Olofsson, Or ...
- Feucht, M.
- Friis, M.
- Heils, A.
- Kjeldsen, M.
- Larsson, K.
- Lehesjoki, A. E.
- Nabbout, R.
- Olsson, Ingrid, ...
- Sander, T.
- Siren, A.
- Robinson, R.
- Rees, M.
- Gardiner, R. M.
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- Articles in the publication
- Epilepsy Res
- By the university
- University of Gothenburg
- Uppsala University
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