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Evaluation of CACNA1H in European patients with childhood absence epilepsy.
Chioza, Barry; Everett, Kate; Aschauer, Harald; Brouwer, Oebele; Callenbach, Petra; Covanis, Athanasios; Dulac, Olivier; Durner, Martina; Eeg-Olofsson, Orvar; Feucht, Martha; Friis, Mogens; Heils, Armin; Kjeldsen, Marianne; Larsson, Katrin; Lehesjoki, Anna-Elina; Nabbout, Rima; Olsson, Ingrid; Sander, Thomas; Sirén, Auli; Robinson, Robert; Rees, Michele; Gardiner, R Mark.
Afiliação
  • Chioza B; Department of Paediatrics and Child Health, Royal Free and University College Medical School, University College London, The Rayne Building, 5 University Street, London WC1E 6JJ, UK.
Epilepsy Res ; 69(2): 177-81, 2006 May.
Article em En | MEDLINE | ID: mdl-16504478
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.
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Base de dados: MEDLINE Assunto principal: Epilepsia Tipo Ausência / Canais de Cálcio Tipo T / Povo Asiático / População Branca / Ligação Genética Limite: Humans Idioma: En Ano de publicação: 2006 Tipo de documento: Article
Buscar no Google
Imprimir
XML
PubMed Links

Base de dados: MEDLINE Assunto principal: Epilepsia Tipo Ausência / Canais de Cálcio Tipo T / Povo Asiático / População Branca / Ligação Genética Limite: Humans Idioma: En Ano de publicação: 2006 Tipo de documento: Article